Jindal Medi Surge

Orthopedic Duo Cage Titanium Spine Implant SpecificationsMaterial:
Manufactured from medical-grade titanium alloy, typically Ti6Al4V or Ti6Al4V ELI.Design:
The Duo Cage is designed for anterior (ALIF), posterior (PLIF), or transforaminal (TLIF) lumbar interbody fusion.Features a versatile design that can be used for multiple approaches to spinal fusion.Open architecture or fenestrated design for bone graft placement and enhanced osseointegration.Available in various shapes such as rectangular or kidney-shaped, depending on the intended approach and anatomical requirements.Dimensions:
Available in multiple sizes to fit different patient anatomies and surgical requirements.Heights typically range from 7mm to 16mm.Lengths and widths vary based on the specific design but usually range from 22mm to 34mm in length and 8mm to 12mm in width.Features:
Textured or serrated surfaces to prevent migration and ensure stability within the intervertebral space.Radiopaque markers for precise intraoperative and postoperative imaging.Various lordotic angles (e.g., 0°, 5°, 10°, 15°) to help restore the natural curvature of the spine and accommodate different anatomical needs.Self-distracting design for ease of insertion and minimal disruption to surrounding tissues.Intended Use:
Designed for use in spinal fusion surgeries to provide stability and support to the lumbar spine.Commonly indicated for degenerative disc disease, spondylolisthesis, and recurrent disc herniation.Sterilization:
Supplied sterile or non-sterile according to manufacturer specifications.If supplied non-sterile, it can be sterilized using standard autoclave methods.Compatibility:
Compatible with various spinal fixation systems, including pedicle screw and rod systems, for comprehensive spinal stabilization.Regulatory Compliance:
Must adhere to international standards such as ISO 13485 for medical devices.Compliance with specific regional regulations like FDA approval (for the USA) or CE marking (for Europe).

Polyaxial Pedicle Screw With Inner Nut Dual Thread Titanium4.DI502.25 4.5 X 25mm4.DI502.26 4.5 X 30mm4.DI502.27 4.5 X 35mm4.DI502.28 4.5 X 40mm4.DI502.29 4.5 X 45mm4.DI502.30 5.5 X 30mm4.DI502.31 5.5 X 35mm4.DI502.32 5.5 X 40mm4.DI502.33 5.5 X 45mm4.DI502.34 5.5 X 50mm4.DI502.35 6.5 X 30mm4.DI502.36 6.5 X 35mm4.DI502.37 6.5 X 40mm4.DI502.38 6.5 X 45mm4.DI502.39 6.5 X 50mm

Here are the general specifications for an Orthopedic Polyaxial Pedicle Screw with Inner Nut and Dual Thread made from Titanium:
Polyaxial Pedicle Screw with Inner Nut Dual Thread TitaniumMaterial:
Titanium (often Ti6Al4V): Known for its high strength, biocompatibility, and resistance to corrosion.Design Features:
Polyaxial Design: Allows the screw head to be angled in multiple directions for improved alignment and fixation flexibility.Inner Nut: Secures the screw in the chosen position and locks it in place against the rod or other fixation devices.Dual Thread: Features two threads on the shaft, which can offer enhanced stability and grip within the pedicle. Typically, this includes:Primary Thread: For secure engagement with the bone.Secondary Thread: Often finer or differently pitched, designed to enhance grip or adjustability.Head Design: Includes a slot or attachment point for connecting to spinal rods or plates.Diameter Options:
Common diameters range from 4.5mm to 6.5mm, but sizes can vary based on specific designs and manufacturer specifications.Length Options:
Available in various lengths, typically ranging from 30mm to 60mm or more, depending on patient needs and anatomical considerations.Indications:
Spinal fixation and stabilizationTreatment of spinal deformities, fractures, or instabilityUtilized in conjunction with rods, plates, and other spinal implants for comprehensive spinal stabilization.Sterilization:
Supplied either sterile or non-sterileCan be sterilized following standard hospital protocols (e.g., autoclaving)Compliance:
Meets international standards for spinal implants, such as ISO 13485 for medical devices.Additional Components:
Locking nutsSpinal rods or plates (for complete spinal fixation systems)Instrumentation for insertion and adjustment

4.SI506 Expandable Cage Titanium4.SI506.08 Ø10mm 20mm X 25mm4.SI506.09 Ø10mm 25mm X 35mm4.SI506.10 Ø10mm 35mm X 55mm4.SI506.11 Ø10mm 55mm X 75mm4.SI506.12 Ø12mm 20mm X 25mm4.SI506.13 Ø12mm 25mm X 35mm4.SI506.14 Ø12mm 35mm X 55mm4.SI506.15 Ø12mm 55mm X 75mm4.SI506.16 Ø14mm 20mm X 25mm4.SI506.17 Ø14mm 25mm X 35mm4.SI506.18 Ø14mm 35mm X 55mm4.SI506.19 Ø14mm 55mm X 75mm4.SI506.20 Ø16mm 20mm X 25mm4.SI506.21 Ø16mm 25mm X 35mm4.SI506.22 Ø16mm 35mm X 55mm4.SI506.23 Ø16mm 55mm X 75mm4.SI506.24 Ø18mm 20mm X 25mm4.SI506.25 Ø18mm 25mm X 35mm4.SI506.26 Ø18mm 35mm X 55mm4.SI506.27 Ø18mm 55mm X 75mm4.SI506.28 Ø20mm 20mm X 25mm4.SI506.29 Ø20mm 25mm X 35mm4.SI506.30 Ø20mm 35mm X 55mm4.SI506.31 Ø20mm 55mm X 75mm

Here are the general specifications for an Orthopedic Expandable Cage made from Titanium, used in spine implants:
Orthopedic Expandable Cage Titanium Spine ImplantMaterial:
Titanium (often Ti6Al4V): Provides high strength, excellent biocompatibility, and resistance to corrosion.Design Features:
Expandable Design: Allows the cage to be expanded after insertion to fit the intervertebral space precisely, providing customizable support and stabilization.Bone Grafting: Often features a structure that allows for the placement of bone graft material or biologics to promote fusion and bone growth.Surface Texture: Typically has a roughened or porous surface to enhance bone ingrowth and improve stability.Shape: May be designed in various shapes, such as cylindrical, box-shaped, or cage-like, to fit different anatomical requirements and surgical needs.Mechanism: The expansion mechanism can vary, including hydraulic, mechanical, or screw-driven systems.Diameter and Dimensions:
Pre-Expansion Diameter: Commonly varies, with dimensions typically ranging from 8mm to 14mm for the initial insertion.Post-Expansion Dimensions: Can expand to fit the intervertebral space, often ranging from 10mm to 20mm or more, depending on the device.Length:
Available in various lengths to match the intervertebral space and patient anatomy, typically ranging from 20mm to 50mm or more.Indications:
Spinal fusion and stabilizationTreatment of degenerative disc disease, spinal fractures, or deformitiesProvides structural support and helps restore disc heightSterilization:
Supplied either sterile or non-sterileCan be sterilized using standard hospital protocols (e.g., autoclaving)Compliance:
Meets international standards for spinal implants, such as ISO 13485 for medical devices.Additional Components:
May include instrumentation for insertion and expansionBone grafting material or biologics (depending on the specific design and surgical requirements)

Orthopedic PLIF Cage Titanium Spine Implant SpecificationsMaterial:
Constructed from medical-grade titanium alloy (commonly Ti6Al4V or Ti6Al4V ELI).Design:
The PLIF (Posterior Lumbar Interbody Fusion) cage is designed to facilitate spinal fusion through a posterior approach.Rectangular or kidney-shaped design to fit the lumbar intervertebral disc space.Open architecture to allow bone graft placement and enhance osseointegration.Dimensions:
Available in various heights, widths, and lengths to suit different patient anatomies and surgical needs.Heights typically range from 8mm to 14mm.Widths typically range from 8mm to 12mm.Lengths typically range from 22mm to 28mm.Features:
Serrated or textured surfaces to prevent migration and enhance stability.Radiopaque markers to assist with intraoperative and postoperative imaging.Multiple lordotic angles (e.g., 0°, 5°, 10°) to help restore the natural curvature of the spine.Intended Use:
Used in spinal fusion procedures to provide support and stability to the lumbar spine.Indicated for conditions such as degenerative disc disease, spondylolisthesis, and recurrent disc herniation.Sterilization:
Supplied sterile or non-sterile, depending on the manufacturer’s specifications.If provided non-sterile, can be sterilized using standard autoclave methods.Compatibility:
Compatible with various spinal fixation systems, including pedicle screw and rod systems.Regulatory Compliance:
Must comply with international standards such as ISO 13485 for medical devices and specific regional regulations like FDA (for the USA) or CE marking (for Europe).

Monoaxial Pedicle Screw With Inner Nut Titanium4.SI501.25 4.5 X 25mm4.SI501.26 4.5 X 30mm4.SI501.27 4.5 X 35mm4.SI501.28 4.5 X 40mm4.SI501.29 4.5 X 45mm4.SI501.30 5.5 X 30mm4.SI501.31 5.5 X 35mm4.SI501.32 5.5 X 40mm4.SI501.33 5.5 X 45mm4.SI501.34 5.5 X 50mm4.SI501.35 6.5 X 30mm4.SI501.36 6.5 X 35mm4.SI501.37 6.5 X 40mm4.SI501.38 6.5 X 45mm4.SI501.39 6.5 X 50mm
Here are the general specifications for an Orthopedic Monoaxial Pedicle Screw with Inner Nut made from Titanium:
Monoaxial Pedicle Screw with Inner Nut TitaniumMaterial:
Titanium (often Ti6Al4V, alloyed for enhanced strength and biocompatibility)Lightweight and corrosion-resistantDesign Features:
Monoaxial Design: Allows for screw fixation in a single plane of motion.Inner Nut: Typically used for adjusting and securing the screw in place.Threaded Shaft: For secure fixation within the pedicle.Head Design: Usually has a slot or attachment point for connecting to rods or other fixation devices.Self-tapping or Self-drilling: Depending on the specific design and application requirements.Diameter Options:
Common diameters range from 4.5mm to 6.5mm, but specific sizes may vary based on the manufacturer.Length Options:
Varies based on anatomical needs and patient specifications, typically ranging from 30mm to 60mm or more.Indications:
Spinal fixation and stabilizationTreatment of spinal deformities, fractures, or instabilityUsed in conjunction with rods and other spinal implants for comprehensive fixation.Sterilization:
Supplied sterile or non-sterileCan be sterilized using standard hospital protocols (autoclaving)Compliance:
Conforms to international standards for spinal implants (e.g., ISO 13485 for medical devices)Additional Components:
Locking nutsRods or plates (for complete spinal fixation systems)Instrumentation for insertion and adjustment

SPINE SURGICAL INSTRUMENT & IMPLANT

Jindal Medi Surge is a CE and ISO Certified leading Manufacturer and Exporter of Surgical and Orthopedic / Orthopaedic Instruments used for Human (Adult and Pediatric) and Veterinary Surgical Procedures. All Products are made from Surgical Grade Stainless Steel, Aluminum, Titanium & Carbon Fiber Only. Our Products are used by Government Institutes, Private Hospitals, Small Clinics, Individual Doctors Worldwide.

For Bulk Order & Customized Listing, kindly message us.
We sell exclusively on our JMS Brand & also Manufacture on OEM basis for various international brands.

Fenestrated Screw Titanium4F.001 5.5 x 30mm4F.002 5.5 x 35mm4F.003 5.5 x 40mm4F.004 6.5 x 35mm4F.005 6.5 x 40mm4F.006 6.5 x 45mm

Here are the general specifications for an Orthopedic Fenestrated Screw made from Titanium, used in spine implants:
Fenestrated Screw Titanium Spine ImplantMaterial:
Titanium (often Ti6Al4V): Offers high strength, biocompatibility, and resistance to corrosion.Design Features:
Fenestrated Design: Features multiple holes or fenestrations (openings) along the screw shaft. This design allows for enhanced bone ingrowth or cement augmentation, improving fixation stability in situations where bone quality is compromised.Threaded Shaft: Provides secure fixation within the pedicle or vertebral body, with a thread pattern designed to maximize grip and stability.Head Design: Typically includes a slot or attachment point for connecting to spinal rods or plates. The head may have a mechanism for secure locking once the screw is positioned.Diameter Options:
Common diameters range from 4.5mm to 6.5mm, but specific sizes can vary based on the manufacturer.Length Options:
Available in various lengths, generally ranging from 30mm to 60mm or more, depending on the anatomical requirements and patient needs.Indications:
Spinal fixation and stabilizationTreatment of spinal deformities, fractures, or instabilityUsed in situations where enhanced stability is needed due to poor bone quality or for additional fixation in complex cases.Sterilization:
Supplied either sterile or non-sterileCan be sterilized using standard hospital protocols (e.g., autoclaving)Compliance:
Meets international standards for spinal implants, such as ISO 13485 for medical devices.Additional Components:
Locking nutsSpinal rods or plates (for complete spinal fixation systems)Instrumentation for insertion and adjustment

The Orthopedic 3.5mm Lateral Mass Screw with Inner Nut Titanium Spine Implant is a specialized screw designed for spinal fixation, particularly in procedures involving the lateral mass of the cervical spine. This screw is typically made from titanium, which is known for its strength, biocompatibility, and resistance to corrosion.
Key Specifications:Diameter: 3.5mmMaterial: Titanium alloy (commonly Ti-6Al-4V, which is a mix of titanium, aluminum, and vanadium)Screw Type: Cannulated or solid screw with threads designed for secure anchorage in bone.Length: Typically available in various lengths, commonly ranging from 10mm to 24mm, depending on the specific anatomical requirements.Inner Nut: The inner nut allows for additional fixation and stability, providing a locking mechanism that prevents screw backout or loosening after installation.Head Design: Low-profile head with a hexagonal or star drive to facilitate easy insertion and removal.Application: Used in posterior cervical spine fixation procedures, especially in cases requiring stabilization of the cervical vertebrae.

A chisel guide for condylar plate orthopedic surgical procedures is a specialized instrument used to ensure the accurate placement and alignment of chisels when preparing the bone for the insertion of a condylar plate. This instrument is crucial for achieving precise cuts and creating the necessary bone surfaces for optimal implant placement. Here’s an overview of its purpose, design, function, compatibility, and sterilization:
PurposeThe chisel guide is used to assist surgeons in positioning and guiding the chisel accurately during orthopedic procedures involving the placement of condylar plates. It ensures that the bone cuts are made at the correct location and angle, which is essential for the proper fit and stability of the implant.
DesignStructure: The guide typically consists of a frame with an adjustable slot or channel that securely holds the chisel. It may include a handle for ease of use.Material: Constructed from surgical-grade stainless steel or other durable, biocompatible materials that can withstand the rigors of surgery and repeated sterilization.Adjustability: The guide often features adjustable components to accommodate different sizes of chisels and to set the desired angle and depth for the cut.Stabilization Features: Some designs include features to stabilize the guide against the bone, ensuring that it remains in place during the cutting process.FunctionGuiding the Chisel: The primary function of the chisel guide is to direct the chisel along a predetermined path, ensuring that the cuts are precise and accurately aligned with the planned placement of the condylar plate.Adjustability: The adjustable components allow the surgeon to customize the guide according to the specific anatomical requirements and the type of condylar plate being used.Stabilization: By holding the chisel in place, the guide minimizes the risk of slippage or deviation during the cutting process, enhancing surgical accuracy.CompatibilityCondylar Plate Systems: The chisel guide must be compatible with the specific condylar plate system being used. This ensures that the cuts are appropriately aligned with the implant.Interchangeability: Some chisel guides are designed to be used with a variety of condylar plate systems, though it is important to verify compatibility with the specific instruments and implants used in the surgery.SterilizationMaterial: The materials used in the chisel guide are suitable for repeated sterilization processes without degrading.Methods: Sterilization is typically performed using autoclaving (steam sterilization) or other approved methods to ensure the instrument is free from contaminants before use.AvailabilityInstrument Sets: The chisel guide is often included in the instrument sets provided by orthopedic implant companies for condylar plate procedures.Surgical Kits: It may also be available as part of specialized surgical kits designed for specific condylar plate operations.SummaryThe chisel guide for condylar plate orthopedic surgical procedures is a vital tool that ensures precise and accurate cuts during bone preparation. Its design allows for the guided placement of the chisel, minimizing the risk of error and enhancing the fit and stability of the condylar plate implant. Adjustability and compatibility with specific condylar plate systems are crucial features, as is the ability to withstand repeated sterilization. Proper use of the chisel guide contributes significantly to the success of orthopedic surgeries involving condylar plates.

Occiput T Plate Titanium Orthopedic Spine Implant SpecificationsMaterial:
Made from medical-grade titanium alloy (commonly Ti6Al4V or Ti6Al4V ELI).Design:
T-shaped plate designed for occipito-cervical fixation in spine surgeries.Multiple holes for screw fixation to provide secure attachment to the occiput and cervical vertebrae.Anatomically contoured to match the curvature of the occiput for better fit and stability.Dimensions:
Available in various sizes to accommodate different patient anatomies and surgical requirements.Common plate lengths range from 30mm to 60mm.Width of the transverse section typically ranges from 10mm to 20mm.Features:
Low-profile design to minimize soft tissue irritation and reduce the risk of complications.Multiple screw holes to allow for flexible and secure fixation points.Screw holes designed to accept standard occipital and cervical screws.Radiopaque markers for precise intraoperative and postoperative imaging.High strength and rigidity to provide stability and support to the occipito-cervical junction.Intended Use:
Used in occipito-cervical fusion procedures to provide stability and support to the occiput and upper cervical spine.Indicated for conditions such as trauma, tumors, degenerative diseases, and congenital anomalies requiring occipito-cervical stabilization.Sterilization:
Supplied sterile or non-sterile, based on manufacturer specifications.If provided non-sterile, they can be sterilized using standard autoclave methods.Compatibility:
Designed to be compatible with standard occipital and cervical screws.Often used in conjunction with rods and other spinal fixation devices for comprehensive stabilization.

Orthopedic TLIF Cage Titanium Spine Implant SpecificationsMaterial:
Made from medical-grade titanium alloy (usually Ti6Al4V or Ti6Al4V ELI).Design:
The TLIF (Transforaminal Lumbar Interbody Fusion) cage is designed to facilitate spinal fusion.It features an anatomical shape to match the lumbar intervertebral disc space.Cages often have an open architecture to allow for bone graft placement and facilitate osseointegration.Dimensions:
Available in various heights and lengths to accommodate different patient anatomies and surgical requirements.Common heights range from 7mm to 15mm.Common lengths range from 22mm to 30mm.Widths typically range from 8mm to 12mm.Features:
Serrated or textured surfaces to prevent migration and ensure stability.Radiopaque markers to aid in intraoperative and postoperative imaging.Multiple lordotic angles (e.g., 0°, 5°, 10°) to help restore the natural curvature of the spine.Intended Use:
Used in spinal fusion procedures to provide support and stability to the lumbar spine.Typically used in cases of degenerative disc disease, spondylolisthesis, or recurrent disc herniation.Sterilization:
Supplied sterile or non-sterile, depending on manufacturer specifications.Can be sterilized using standard autoclave methods if provided non-sterile.Compatibility:
Compatible with various spinal fixation systems, including pedicle screw and rod systems.Regulatory Compliance:
Must comply with international standards such as ISO 13485 for medical devices and specific regional regulations like FDA (for the USA) or CE marking (for Europe).

14mm Anterior Cervical Fusion Cage Peek 138124.005 5 MM138124.006 6 MM138124.007 7 MM138124.008 8 MM 16mm Anterior Cervical Fusion Cage Peek 138125.005 5 MM138125.006 6 MM138125.007 7 MM138125.008 8 MMThe Orthopedic Anterior Cervical Fusion Cage PEEK Spine Implant is designed for use in Anterior Cervical Discectomy and Fusion (ACDF) procedures. This cage is placed in the cervical intervertebral space after disc removal to restore disc height, maintain spinal alignment, and promote fusion between the vertebral bodies.
Key Specifications:Material:
PEEK (Polyether Ether Ketone): A high-performance polymer known for its strength, biocompatibility, and radiolucency. PEEK does not interfere with imaging modalities like X-rays, CT scans, or MRIs, allowing for clear postoperative imaging.Design:
Shape: Typically rectangular or kidney-shaped to fit the cervical intervertebral space.Size: Available in various heights and footprints to accommodate different patient anatomies and surgical requirements.Lordotic Angle: Often comes in different lordotic angles (e.g., 0°, 7°, 12°) to help restore the natural cervical curvature and maintain sagittal balance.Surface Texture: The surface may be textured or have a roughened finish to enhance bone integration and prevent migration of the implant.Hollow Center: The cage has a hollow center designed to be filled with autograft, allograft, or bone substitute material, which facilitates bone growth through and around the cage, leading to fusion.Endplate Design: The endplates of the cage may have teeth or ridges to ensure secure placement against the vertebral bodies and minimize the risk of migration.Radiopaque Markers:
Markers: Radiopaque markers are often integrated into the PEEK cage to allow for accurate visualization and positioning verification under X-ray or fluoroscopy during and after surgery.Applications:Anterior Cervical Discectomy and Fusion (ACDF):Procedure: The implant is used in ACDF procedures, where it is inserted into the disc space after the removal of a degenerated or herniated cervical disc. The cage helps restore disc height and maintains spinal stability while the bone graft inside the cage facilitates fusion between the adjacent vertebrae.Indications: Common indications for using an anterior cervical fusion cage include cervical disc herniation, degenerative disc disease, spinal stenosis, and spondylosis, where stabilization and fusion of the cervical spine are necessary.

Cervical Impact Fusion Cage 16mm Titanium Orthopedic Spine Implant SpecificationsMaterial:
Made from medical-grade titanium alloy (commonly Ti6Al4V or Ti6Al4V ELI).Design:
Specifically designed for cervical interbody fusion procedures.Impact-type cage to be inserted between the cervical vertebrae for stabilization and fusion.Height of 16mm to accommodate specific anatomical requirements.Dimensions:
Height: 16mm.Width and depth: Varies depending on the specific design, typically ranging from 12mm to 16mm in width and 10mm to 14mm in depth.Shape: Often designed in a wedge or cylindrical shape to fit the intervertebral space snugly.Features:
Surface texture designed to promote bone in-growth and stability, often featuring a roughened or porous surface.Open architecture with large central cavities to allow for bone graft placement, facilitating fusion between vertebrae.Anterior and posterior markers to aid in proper alignment and positioning during implantation.Radiopaque markers for precise intraoperative and postoperative imaging.High strength and stiffness to maintain disc height and alignment while the fusion occurs.Low-profile design to minimize soft tissue irritation and reduce the risk of complications.Intended Use:
Used in cervical spinal fusion procedures to provide stability and support to the cervical spine.Commonly indicated for conditions such as degenerative disc disease, cervical spondylosis, trauma, and spinal deformities.Sterilization:
Supplied sterile or non-sterile, based on manufacturer specifications.If provided non-sterile, they can be sterilized using standard autoclave methods.Compatibility:
Designed to be used with other spinal fixation devices and instruments, such as anterior cervical plates and screws, to ensure comprehensive stabilization and support.Regulatory Compliance:
Must comply with international standards such as ISO 13485 for medical devices.Compliance with specific regional regulations like FDA approval (for the USA) or CE marking (for Europe).

The Orthopedic 120° Angled Blade Plate DCP (Dynamic Compression Plate) Titanium Surgical Implant is a highly specialized orthopedic device designed to provide robust and precise fixation for complex fractures, particularly in anatomically challenging regions such as the proximal femur and tibia. Crafted from premium-grade titanium, this implant offers exceptional strength, biocompatibility, and corrosion resistance, making it an ideal choice for facilitating optimal bone healing and patient recovery.
Key FeaturesMaterial: Titanium Alloy (Ti-6Al-4V)
Biocompatibility: Minimizes adverse tissue reactions, ensuring compatibility with the human body.Corrosion Resistance: Resistant to bodily fluids, reducing the risk of implant degradation.Strength-to-Weight Ratio: Provides robust mechanical support without adding excessive weight, enhancing patient comfort and mobility.Radiolucency: Allows for clear postoperative imaging, aiding in monitoring bone healing without significant artifact interference.Design: 120° Angled Blade Plate
Fixed Angle: The 120° configuration is engineered to match the natural curvature of bones like the proximal femur, ensuring optimal anatomical alignment.Blade Integration: The angled blade serves as an anchoring mechanism within the bone, providing enhanced mechanical stability and preventing rotational displacement of bone fragments.Dynamic Compression: Facilitates controlled compression at the fracture site, promoting faster and more reliable bone healing by drawing bone fragments together.Dynamic Compression Plate (DCP) Technology
Compression Mechanism: Allows for the application of compressive forces across the fracture site, enhancing stability and promoting bone union.Micromotion Accommodation: Supports micromotion at the fracture site, which is beneficial for bone remodeling and healing.Screw Configuration
Multiple Screw Holes: Equipped with several holes to accommodate both locking and non-locking screws, offering versatile fixation options tailored to specific fracture types and bone quality.Locking Capabilities: Compatible with locking screws that provide angular stability, particularly advantageous in osteoporotic or comminuted fractures.Optimal Screw Placement: Designed to allow precise screw placement, maximizing fixation strength and minimizing interference with surrounding tissues.Sizes and Variants
Multiple Plate Lengths: Available in various lengths (typically ranging from 6 cm to 20 cm) to accommodate different bone sizes and fracture patterns.Blade Length Options: Offered in different blade lengths (commonly between 3 cm to 6 cm) to suit varying anatomical requirements and surgical needs.Hole Configuration: Designed with a combination of locking and non-locking screw holes to enhance versatility in surgical applications.Sterilization and Packaging
Sterile Packaging: Each implant is individually sterilized and packaged to maintain aseptic conditions until use.User-Friendly Packaging: Designed for easy identification and accessibility during surgical procedures, streamlining the surgical workflow.

Semi Tubular Plate For 3.5mm Screw Titanium4143T.1022 Holes4143T.1033 Holes4143T.1044 Holes4143T.1055 Holes4143T.1066 Holes4143T.1077 Holes4143T.1088 Holes4143T.1099 Holes4143T.11010 Holes4143T.11212 HolesThe Orthopedic Semi Tubular Plate for 3.5mm screws, made from Titanium, is a specialized implant designed for the internal fixation of fractures, particularly in bones requiring partial support along their curvature. The semi-tubular design is optimized to conform to the natural shape of the bone, offering secure and stable fixation.Specifications:Material: Titanium (commonly Ti-6Al-4V ELI Grade)Plate Thickness: Designed to accommodate 3.5mm screwsDesign:Shape: Semi-tubular, meaning the plate has a curved profile to match the contour of the bone.Number of Holes: Varies depending on the length of the plate (typically ranges from 4 to 12 holes).Hole Diameter: Specifically designed for 3.5mm cortical screws.Curvature: The semi-tubular design allows the plate to fit naturally along the curvature of long bones, such as the radius, ulna, or metatarsals.Features:Biocompatibility: Titanium is highly biocompatible, minimizing the risk of allergic reactions and promoting better integration with bone tissue.Corrosion Resistance: Titanium provides superior resistance to corrosion, ensuring the implant remains intact and effective over the long term.Lightweight: Titanium is known for its high strength-to-weight ratio, making the implant strong yet lightweight, which reduces the load on the bone.Semi-Tubular Design: The plate\'s curvature conforms closely to the bone surface, providing better stability and reducing the risk of soft tissue irritation.Pre-Contoured: Often pre-shaped to match the bone\'s natural anatomy but can be adjusted during surgery as needed.Smooth Edges: Designed with smooth, rounded edges to minimize soft tissue irritation.Application:Indications:Ideal for fixation of fractures in smaller or curved bones, such as the radius, ulna, or metatarsals.Suitable for cases where the bone’s natural contour must be maintained for proper healing.Surgical Use:Can be utilized in both open and closed reduction techniques.Commonly used in orthopedic trauma surgeries requiring stabilization of bones with natural curvature.Benefits:Enhanced Stability: The semi-tubular shape provides a secure fit along the bone’s contour, ensuring stable fixation and minimizing the risk of displacement.Maintains Bone Contour: Helps preserve the natural shape of the bone, which is crucial for functional recovery.Lightweight Strength: Titanium’s high strength-to-weight ratio ensures that the implant is strong but does not add unnecessary weight, reducing patient discomfort.Long-Term Durability: Titanium’s excellent biocompatibility and corrosion resistance make it suitable for long-term implantation.Reduced Soft Tissue Irritation: Smooth edges and a contoured design help minimize irritation to surrounding soft tissues, promoting faster recovery.The Orthopedic Semi Tubular Plate for 3.5mm screws, made from Titanium, is an advanced implant solution that provides effective fixation and stability for fractures in curved bones. Its design and material properties make it an excellent choice for orthopedic surgeons aiming for optimal patient outcomes.

A single-hole 50mm distractor in orthopedic surgery is a specialized instrument used primarily for bone realignment and stabilization. Here’s an overview of what this instrument entails and its application:
Single-Hole 50mm Distractor: Overview and UsageDesign and ConstructionMaterial: Typically made of high-quality stainless steel for durability, sterilization, and corrosion resistance.Structure: The distractor consists of a central body with a single hole and a mechanism (often a screw) for adjusting the distraction length. The hole allows for the passage of screws or pins to secure the distractor to the bone.FeaturesAdjustability: The central screw mechanism allows for precise adjustment of the distraction length, which is crucial for achieving optimal bone alignment.Stability: Provides stable fixation during the distraction process, minimizing the risk of bone fragment displacement.Versatility: Suitable for various orthopedic procedures where controlled distraction is necessary, such as fractures, osteotomies, or corrective surgeries.Application in Orthopedic SurgeryPreparation:The surgical site is prepared, and the patient is positioned appropriately under anesthesia.Attachment of Distractor:Placement: The distractor is positioned at the desired location on the bone surface.Securing: Screws or pins are inserted through the hole in the distractor and into the bone to secure it firmly in place.Distraction:Adjustment: The central screw is turned to gradually separate bone fragments or create the desired space between bone ends, facilitating controlled realignment.Monitoring: Throughout the distraction process, the surgeon monitors the alignment of bone fragments or bone ends to ensure they are properly positioned.Completion:Once the desired distraction and alignment are achieved, additional fixation devices such as screws, plates, or rods may be used to stabilize the bone fragments or bone ends.The distractor is carefully removed after achieving the desired surgical outcome.Advantages of Using a Single-Hole 50mm DistractorPrecision: Allows for precise and controlled realignment of bone fragments or bone ends, promoting optimal healing.Stability: Provides stable fixation during the distraction process, reducing the risk of fragment displacement.Efficiency: Facilitates efficient surgical procedures by aiding in accurate bone alignment and stabilization, potentially reducing surgical time and patient trauma.Maintenance and SterilizationCleaning: After each use, the distractor must be thoroughly cleaned to remove biological material or debris.Sterilization: The instrument must undergo sterilization according to standard surgical protocols to ensure it is safe for reuse.ConclusionA single-hole 50mm distractor is a crucial instrument in orthopedic surgery, enabling surgeons to perform controlled bone distraction for various procedures aimed at bone realignment and stabilization. Its design and functionality support precise surgical outcomes and efficient patient care. Proper maintenance and sterilization are essential to ensure the instrument's effectiveness and safety in surgical settings.
If you need more specific information, including models or purchasing options for single-hole 50mm distractors, please let me know!

A skin hook with two prongs is a specialized surgical instrument used in various surgical fields, including orthopedic, plastic, and general surgery, to retract and hold skin and other delicate tissues. Here are the key details about this instrument:
Description:Function: The two-prong skin hook is designed to gently retract skin and soft tissues, providing surgeons with enhanced visibility and access to the surgical site.Design: Features two sharp, evenly spaced prongs at the end of a handle. These prongs are used to securely grip and retract the tissue with minimal trauma.Features:Material:
Prongs and Shaft: Typically made of high-quality surgical-grade stainless steel for durability, resistance to corrosion, and ease of sterilization.Handle: Usually crafted from stainless steel, but it can also be designed with an ergonomic, textured grip to enhance control and comfort during use.Prong Design:
Sharpness: The two prongs are sharp enough to easily penetrate the skin with minimal damage, providing effective retraction without tearing the tissue.Spacing: The prongs are evenly spaced to distribute the retraction force across the tissue, reducing the risk of localized damage.Handle Design:
Ergonomics: The handle is designed to provide a comfortable and secure grip, reducing hand fatigue during prolonged use.Textured Surface: Often features a textured or knurled handle to prevent slipping and improve control, especially in a moist surgical environment.Sterilization:
Compatibility: The instrument is designed to withstand standard sterilization procedures, including autoclaving, ensuring it can be safely reused.Applications:Orthopedic Surgery: Used to retract skin and soft tissues during procedures such as joint replacements, fracture repairs, and other orthopedic surgeries.Plastic Surgery: Employed in procedures requiring precise manipulation of the skin, such as reconstructive surgeries and cosmetic enhancements.General Surgery: Utilized in a wide range of surgical procedures to hold back skin and soft tissues, providing better access to the underlying structures.ENT Surgery: Commonly used in ear, nose, and throat surgeries to manage delicate tissues with precision.Neurosurgery: Sometimes used in spinal and cranial procedures where delicate retraction of tissue is required.Maintenance:Cleaning: Post-operative cleaning is essential to remove biological debris. This includes manual cleaning and possibly ultrasonic cleaning for thorough decontamination.Inspection: Regular inspection for signs of wear, corrosion, or damage is necessary to maintain the instrument's effectiveness and safety.Sterilization: Must be sterilized using autoclaving or chemical sterilants according to the manufacturer's guidelines to ensure it is pathogen-free before reuse.Advantages of a Two-Prong Skin Hook:Secure Retraction: The two-prong design provides secure and stable retraction, distributing the force more evenly compared to a single prong, reducing tissue trauma.Improved Visibility: By securely holding the skin and soft tissues, the two-prong skin hook offers better visibility and access to the surgical site.Control and Precision: The ergonomic design of the handle and the configuration of the prongs allow the surgeon to manipulate the instrument with great control and precision.The two-prong skin hook is a valuable tool in the surgical toolkit, providing reliable and gentle tissue retraction for a variety of surgical procedures. Its design ensures precision, control, and minimal tissue damage, contributing to successful surgical outcomes.

Anterior Cervical Plate 4 Holes Titanium4.SI512.21 21mm4.SI512.22 22mm4.SI512.221 23mm4.SI512.23 24mm4.SI512.231 25mm4.SI512.24 26mm4.SI512.241 27mm4.SI512.25 28mm4.SI512.26 30mmOrthopedic Anterior Cervical Plate with 4 Holes Titanium Spine Implant SpecificationsMaterial:
Made from medical-grade titanium alloy (commonly Ti6Al4V or Ti6Al4V ELI).Design:
Anterior cervical plate designed for spinal fixation and stabilization.Features 4 holes to accommodate screws for secure fixation to the cervical vertebrae.Anatomically contoured to match the curvature of the cervical spine.Low-profile design to minimize soft tissue irritation and reduce the risk of dysphagia.Dimensions:
Length: Varies to accommodate different levels of fusion, typically ranging from 20mm to 40mm.Width: Approximately 15mm to 20mm.Thickness: Typically around 2mm to 3mm.Features:
Screw holes with variable angle capabilities to allow for optimal screw placement and purchase in the vertebral bodies.Locking mechanisms such as locking caps or screws to prevent screw back-out and ensure stability.Radiopaque markers or indicators for precise intraoperative and postoperative imaging.Slots or grooves to facilitate bone grafting and enhance fusion.Intended Use:
Used in anterior cervical spinal fusion procedures to provide stability and support to the cervical spine.Commonly indicated for conditions such as degenerative disc disease, trauma, tumors, and deformities.Sterilization:
Supplied sterile or non-sterile, based on manufacturer specifications.Can be sterilized using standard autoclave methods if provided non-sterile.Compatibility:
Designed to be compatible with specific anterior cervical screws, typically of varying lengths and diameters to match patient anatomy and surgical requirements.Regulatory Compliance:
Must comply with international standards such as ISO 13485 for medical devices.Specific regional regulations like FDA approval (for the USA) or CE marking (for Europe) must be met.

Orthopedic Screws for Cervical Cage with Plate Titanium Spine Implant SpecificationsMaterial:
Constructed from medical-grade titanium alloy (commonly Ti6Al4V or Ti6Al4V ELI).Design:
Specifically designed for use with zero-profile cervical cage and plate systems.Self-tapping and/or self-drilling tips to facilitate easy insertion and secure anchoring in the vertebral bodies.Screws are typically low-profile to maintain the zero-profile design of the implant.Dimensions:
Available in various diameters and lengths to match the specific requirements of the cervical cage and plate system.Common diameters range from 3.5mm to 4.5mm.Lengths typically range from 10mm to 20mm.Features:
Threaded design to provide secure fixation in the vertebral bone.Variable-angle or fixed-angle designs to allow for optimal screw placement and alignment with the cage and plate.Head designs that ensure secure locking within the plate, often featuring locking mechanisms such as a polyaxial head or a locking cap.Radiopaque markers to assist with precise intraoperative and postoperative imaging.Intended Use:
Used in cervical spinal fusion procedures in conjunction with a cervical cage with an integrated plate.Provides immediate stability and support to the cervical spine by anchoring the cage and plate to the vertebrae.Indicated for conditions such as degenerative disc disease, cervical spondylosis, trauma, and recurrent disc herniation.Sterilization:
Supplied sterile or non-sterile, based on manufacturer specifications.If provided non-sterile, they can be sterilized using standard autoclave methods.Compatibility:
Designed to be compatible with specific zero-profile cervical cage and plate systems.Ensure compatibility with the dimensions and locking mechanisms of the corresponding cage and plate.Regulatory Compliance:
Must adhere to international standards such as ISO 13485 for medical devices.Compliance with specific regional regulations like FDA approval (for the USA) or CE marking (for Europe).

Reduction Polyaxial Screw Titanium4.SI503.31 4.5 X 30mm4.SI503.32 4.5 X 35mm4.SI503.33 4.5 X 40mm4.SI503.34 4.5 X 45mm4.SI503.35 4.5 X 50mm4.SI503.36 5.5 X 30mm4.SI503.37 5.5 X 35mm4.SI503.38 5.5 X 40mm4.SI503.39 5.5 X 45mm4.SI503.40 5.5 X 50mm4.SI503.41 6.5 X 30mm4.SI503.42 6.5 X 35mm4.SI503.43 6.5 X 40mm4.SI503.44 6.5 X 45mm4.SI503.45 6.5 X 50mm
Here are the general specifications for an Orthopedic Reduction Polyaxial Screw made from Titanium, used in spine implants:
Reduction Polyaxial Screw TitaniumMaterial:
Titanium (often Ti6Al4V): Known for its high strength, excellent biocompatibility, and resistance to corrosion.Design Features:
Polyaxial Design: Allows for multi-directional angling of the screw head, providing flexibility in alignment and fixation.Reduction Capability: Designed to aid in reducing (aligning) spinal deformities or fractures. This usually includes mechanisms to adjust and correct spinal alignment.Threaded Shaft: Features a thread pattern optimized for secure fixation within the pedicle or vertebral body.Head Design: Includes a slot or attachment point for connecting to spinal rods or plates. Often features an inner mechanism (such as a set screw) to lock the head in place once the desired alignment is achieved.Diameter Options:
Common diameters range from 4.5mm to 6.5mm, but sizes can vary based on specific design and manufacturer specifications.Length Options:
Available in various lengths, typically ranging from 30mm to 60mm or more, depending on the patient’s anatomy and surgical needs.Indications:
Spinal fixation and stabilizationTreatment of spinal deformities, fractures, or instabilityUsed in conjunction with rods, plates, and other spinal implants to achieve proper alignment and stabilization of the spine.Sterilization:
Supplied sterile or non-sterileCan be sterilized using standard hospital protocols (e.g., autoclaving)Compliance:
Conforms to international standards for spinal implants, such as ISO 13485 for medical devices.Additional Components:
Locking nutsSpinal rods or plates (for complete spinal fixation systems)Instrumentation for insertion, adjustment, and alignment

Orthopedic Occipital Plate Bone Screw Titanium Spine Implant SpecificationsMaterial:
Made from medical-grade titanium alloy (commonly Ti6Al4V or Ti6Al4V ELI).Design:
Bone screws designed for use with occipital plates in spinal surgeries.Specifically intended for secure fixation to the occipital bone and the cervical spine.Dimensions:
Diameter: Commonly ranges from 3.5mm to 4.5mm.Length: Typically ranges from 10mm to 30mm, depending on the patient's anatomy and the surgical requirements.Head Design: Often has a low-profile head or a specific shape to fit within the occipital plate and minimize soft tissue irritation.Features:
Threaded Design: Provides secure anchorage in the occipital bone.Self-Tapping or Self-Drilling: Facilitates easier insertion without the need for pre-drilling, depending on the specific design.Radiopaque Markers: Allow for precise intraoperative and postoperative imaging.Locking Mechanism: Some designs feature a locking mechanism to secure the screw in place within the occipital plate.Intended Use:
Used in conjunction with occipital plates for stabilization and fusion in the occipito-cervical junction.Commonly indicated for conditions such as trauma, tumors, degenerative diseases, or congenital anomalies requiring occipital fixation.Sterilization:
Supplied sterile or non-sterile, based on manufacturer specifications.If provided non-sterile, can be sterilized using standard autoclave methods.Compatibility:
Designed to be compatible with specific occipital plates and other spinal fixation devices.Often used in conjunction with rods, plates, and screws in comprehensive spinal stabilization systems.Regulatory Compliance:
Must comply with international standards such as ISO 13485 for medical devices.Compliance with specific regional regulations like FDA approval (for the USA) or CE marking (for Europe).

Orthopedic DHS Barrel Plate with DCP Holes (125°) – Material: SS316LThe Dynamic Hip Screw (DHS) Barrel Plate with DCP Holes is an advanced orthopedic implant designed for fixation of proximal femur fractures, including intertrochanteric and subtrochanteric fractures. This implant features a 125° angled barrel and Dynamic Compression Plate (DCP) holes to provide strong and stable fixation.
Key FeaturesMaterial: SS316L
Manufactured from medical-grade Stainless Steel 316L:High corrosion resistance for long-term implantation.Biocompatible to minimize tissue reactions.Durable and strong to withstand load-bearing applications.Barrel Design (125°)
Fixed-angle barrel optimized for proximal femur fixation.Ensures precise alignment of the dynamic hip screw and femoral neck.Dynamic Compression Plate (DCP) Holes
Enables compression across the fracture site, promoting stable bone healing.Compatible with standard cortical screws for fixation.Low-Profile Design
Minimizes soft tissue irritation post-implantation.Available in Multiple Lengths
Offered in various configurations to accommodate different fracture patterns and patient anatomies.Indications for UseIntertrochanteric Femur Fractures
Stabilizes fractures occurring between the greater and lesser trochanter.Subtrochanteric Femur Fractures
Provides fixation in fractures extending below the lesser trochanter.Proximal Femur Fixation in Osteoporotic Bone
Ideal for fractures in weakened bone where angular stability is critical.Pathological Fractures
Used in cases involving bone affected by disease, such as tumors or metabolic conditions.AdvantagesOptimal Alignment
125° barrel ensures precise positioning of the dynamic hip screw in the femoral neck, promoting better load distribution.Enhanced Stability
DCP holes allow compression across the fracture site, reducing movement and ensuring proper healing.Durability
SS316L material ensures the implant remains robust under high load conditions.Versatility
Can be used for various proximal femur fracture patterns.Reduced Tissue Irritation
Low-profile design prevents postoperative discomfort and soft tissue complications.Surgical TechniquePreoperative Planning
Assess the fracture with imaging (e.g., X-ray, CT scan) to select the appropriate barrel angle (125°) and plate length.Plate and Screw Insertion
Position the barrel plate along the lateral femur.Insert the dynamic hip screw through the barrel to stabilize the femoral neck.Fixation with DCP Holes
Secure the plate to the femur using cortical screws through the DCP holes.Apply compression across the fracture site for enhanced stability.Postoperative Imaging
Verify implant alignment and fixation with imaging.Applications in Orthopedic Trauma SurgeryThe DHS Barrel Plate with DCP Holes is an essential implant in managing proximal femoral fractures. It provides a combination of angular stability, compression, and robust fixation, making it suitable for a variety of clinical scenarios, including fractures in osteoporotic bone.For more details on dimensions, screw compatibility, or specific surgical guidelines, feel free to ask!

The Orthopedic T Plate 4.5mm made from Titanium is a specialized surgical implant designed for the fixation of fractures, particularly near joint surfaces or at the ends of long bones. Its "T" shape and titanium material offer superior strength, biocompatibility, and reduced weight, making it ideal for complex fractures in regions like the distal tibia or humerus.
Specifications:Material: Titanium, known for its excellent biocompatibility, lightweight, corrosion resistance, and reduced risk of allergic reactions. It integrates well with bone (osseointegration), promoting better healing.
Screw Compatibility: Designed for use with 4.5mm cortical screws, providing strong and stable fixation.
Plate Type:
T-Plate: The T-shaped design is ideal for fractures at the ends of long bones, particularly in areas like the distal tibia, distal humerus, or other joint regions. The wider "T" section allows for additional screws to be placed near the bone ends, providing increased stabilization.Design Features:
Dynamic Compression: The shaft of the plate has oval holes, enabling dynamic compression across the fracture when screws are tightened, promoting bone healing by reducing the fracture gap.Angled Design: The wider head (the top of the "T") provides multiple points of screw insertion, offering enhanced stability at the epiphyseal (end) regions of bones.Available Lengths: Comes in various lengths and hole configurations to accommodate different fracture types and bone sizes, typically ranging from 3 to 8 holes in the shaft and 3 to 4 holes in the "T" portion.Thickness: The plate is approximately 4.5mm thick, providing strength for load-bearing bones while maintaining a low profile to minimize soft tissue irritation.
Weight: Titanium is significantly lighter than stainless steel, reducing patient discomfort and making it an excellent choice for long-term implants.
Applications:Distal Tibia and Distal Humerus Fractures: Commonly used for fractures at or near joint surfaces, such as the ankle or elbow, where the "T" shape provides extra support.Epiphyseal and Metaphyseal Fractures: Effective for fractures near the ends of bones, ensuring secure fixation in areas where fractures are more prone to displacement.Articular and Complex Fractures: Especially beneficial in joint-related fractures where additional stability is required to maintain bone alignment.This 4.5mm T-Plate made of Titanium is preferred in cases where lightweight, high strength, and superior biocompatibility are crucial for patient recovery. It ensures reliable fracture stabilization with minimal impact on soft tissues, making it an optimal choice for orthopedic surgeries in critical bone regions.

Spine Rod 3mm Dia. Titanium4.SI504.60 60mm4.SI504.61 70mm4.SI504.62 80mm4.SI504.63 120mm4.SI504.64 150mm4.SI504.65 200mm4.SI504.66 250mm4.SI504.67 350mm4.SI504.68 420mm

Here are the general specifications for an Orthopedic Spine Rod with a diameter of 3mm, made from Titanium:
Orthopedic Spine Rod 3mm Diameter TitaniumMaterial:
Titanium (often Ti6Al4V): Provides high strength, excellent biocompatibility, and resistance to corrosion.Diameter:
3mm: The rod has a diameter of 3mm, which is relatively thin and may be used in specific cases requiring minimal rod size.Length:
Varies based on surgical requirements and anatomical needs. Common lengths range from 100mm to 300mm or more, depending on the application.Design Features:
Straight or Curved: Depending on the specific needs of the spinal fixation, rods may be straight or pre-bent to conform to spinal curves.Surface Finish: Typically smooth to reduce irritation and improve biocompatibility.Compatibility: Designed to work with various spinal fixation systems, including screws, plates, and connectors.Indications:
Spinal fixation and stabilizationUsed in conjunction with pedicle screws, plates, and other implants to stabilize and align the spine.Commonly used in spinal deformity correction, trauma, or degenerative conditions.Sterilization:
Supplied either sterile or non-sterileCan be sterilized using standard hospital protocols (e.g., autoclaving)Compliance:
Conforms to international standards for spinal implants, such as ISO 13485 for medical devices.Additional Components:
May include connectors or clamps for attachment to spinal screws or plates.Instrumentation for insertion and adjustment.

Reduction Monoaxial Screw Titanium4M.SI503.31 4.5 X 30mm4M.SI503.32 4.5 X 35mm4M.SI503.33 4.5 X 40mm4M.SI503.34 4.5 X 45mm4M.SI503.35 4.5 X 50mm4M.SI503.36 5.5 X 30mm4M.SI503.37 5.5 X 35mm4M.SI503.38 5.5 X 40mm4M.SI503.39 5.5 X 45mm4M.SI503.40 5.5 X 50mm4M.SI503.41 6.5 X 30mm4M.SI503.42 6.5 X 35mm4M.SI503.43 6.5 X 40mm4M.SI503.44 6.5 X 45mm4M.SI503.45 6.5 X 50mm
Here are the general specifications for a Reduction Monoaxial Screw made from Titanium, used in orthopedic spine implants:
Reduction Monoaxial Screw TitaniumMaterial:
Titanium (often Ti6Al4V): Offers high strength, excellent biocompatibility, and resistance to corrosion.Design Features:
Monoaxial Design: Allows for fixation in a single plane of motion, typically with a fixed angle.Reduction Capability: Designed to aid in the reduction (alignment) of spinal deformities or fractures, often featuring mechanisms to adjust the position of the screw to correct alignment.Threaded Shaft: Provides secure fixation within the pedicle or vertebral body. Thread patterns may vary for enhanced stability.Head Design: Typically includes a slot or attachment point to connect with spinal rods or plates. The head may be designed for easy attachment and adjustment.Diameter Options:
Common diameters range from 4.5mm to 6.5mm, but sizes may vary depending on specific design and manufacturer.Length Options:
Available in various lengths, typically ranging from 30mm to 60mm or more, depending on patient needs and anatomical considerations.Indications:
Spinal fixation and stabilizationTreatment of spinal deformities, fractures, or instabilityUsed to achieve proper alignment and reduction in conjunction with rods, plates, and other spinal implants.Sterilization:
Supplied either sterile or non-sterileCan be sterilized using standard hospital protocols (e.g., autoclaving)Compliance:
Meets international standards for spinal implants, such as ISO 13485 for medical devices.Additional Components:
Locking nutsSpinal rods or plates (for complete spinal fixation systems)Instrumentation for insertion, adjustment, and reduction

The Orthopedic 3.5mm Dynamic Compression Plate (DCP) made from SS316L is a surgical implant used for internal fixation of fractures. The DCP design allows for dynamic compression of the fracture site, promoting better healing. Here are the general specifications and features:
Specifications:Material: Stainless Steel 316L (SS316L)Plate Thickness: 3.5mmNumber of Holes: Varies (commonly available with 4, 6, 8, 10, 12, or more holes, customizable)Length: Varies depending on the number of holes, typically ranging from 50mm to 200mm or moreHole Diameter: Designed to accommodate 3.5mm cortical screwsDesign:Dynamic Compression Plate (DCP): Features specially shaped holes that allow for dynamic compression at the fracture site as screws are inserted eccentrically.Pre-Contoured: Some versions may be pre-contoured to match the anatomy of the bone, while others may require bending during surgery.Rounded Edges: Designed to minimize soft tissue irritation.Features:Corrosion Resistance: Made from SS316L, which is highly resistant to corrosion, making it suitable for long-term implantation.Biocompatibility: SS316L is biocompatible, reducing the risk of adverse tissue reactions.Dynamic Compression: The plate's design allows for the application of compression at the fracture site during screw insertion, which promotes better healing by ensuring close contact between bone fragments.Versatility: Can be used in a variety of bones, including the radius, ulna, fibula, and small long bones.Application:Indications:Used primarily in the fixation of fractures in small bones, such as the forearm (radius and ulna), fibula, or other small long bones.Suitable for both simple and complex fractures where compression of the fracture site is desired.Surgical Use:Can be used for both open and closed fracture fixation.Often used in conjunction with other fixation devices like lag screws for added stability.Benefits:Enhanced Healing: By providing dynamic compression, the DCP helps promote faster and more effective bone healing.Stability: The plate offers solid fixation, reducing the risk of fracture displacement during healing.Customizability: Available in various lengths and hole configurations to match the specific needs of the fracture and patient anatomy.The 3.5mm DCP Plate made from SS316L is widely used in orthopedic surgery for its reliability, strength, and ability to facilitate dynamic compression at the fracture site, promoting optimal healing outcomes.

Orthopedic Anterior Cervical Bone Screw Titanium Spine Implant SpecificationsMaterial:
Made from medical-grade titanium alloy (commonly Ti6Al4V or Ti6Al4V ELI).Design:
Specifically designed for use with anterior cervical plating systems.Self-tapping or self-drilling tips to facilitate easy insertion and secure anchoring in the vertebral bodies.Variable angle and fixed angle options to provide flexibility in screw placement and alignment with the plate.Dimensions:
Available in various diameters and lengths to accommodate different patient anatomies and surgical requirements.Common diameters range from 3.5mm to 4.5mm.Lengths typically range from 10mm to 20mm.Features:
Threaded design to provide secure fixation in the vertebral bone.Screw head designed to lock securely within the cervical plate, often featuring locking mechanisms such as a polyaxial head or a locking cap.Radiopaque markers to assist with precise intraoperative and postoperative imaging.Low-profile head design to minimize soft tissue irritation and reduce the risk of dysphagia.High fatigue strength to withstand the mechanical stresses of the cervical spine.Intended Use:
Used in anterior cervical spinal fusion procedures in conjunction with an anterior cervical plate.Provides immediate stability and support to the cervical spine by anchoring the plate to the vertebrae.Indicated for conditions such as degenerative disc disease, cervical spondylosis, trauma, and recurrent disc herniation.Sterilization:
Supplied sterile or non-sterile, based on manufacturer specifications.If provided non-sterile, they can be sterilized using standard autoclave methods.Compatibility:
Designed to be compatible with specific anterior cervical plates, typically of the same manufacturer or designed for universal compatibility.Regulatory Compliance:
Must comply with international standards such as ISO 13485 for medical devices.Compliance with specific regional regulations like FDA approval (for the USA) or CE marking (for Europe).

Cervical Cage Titanium4.SI511 5.5mm4.SI512 6.5mm4.SI513 7.5mm4.SI514 8.5mm4.SI515 9.5mmOrthopedic Cervical Cage Titanium Spine Implant SpecificationsMaterial:
Constructed from medical-grade titanium alloy (commonly Ti6Al4V or Ti6Al4V ELI).Design:
Designed for anterior cervical interbody fusion (ACIF).Anatomically shaped to fit the cervical vertebral space.Open architecture or fenestrated design for bone graft placement to enhance osseointegration.Available in various shapes such as rectangular, trapezoidal, or lordotic to match patient anatomy.Dimensions:
Available in various heights, widths, and lengths to accommodate different patient anatomies and surgical needs.Heights typically range from 5mm to 12mm.Widths usually range from 12mm to 17mm.Lengths typically range from 12mm to 16mm.Features:
Textured or serrated surfaces to prevent migration and enhance stability.Radiopaque markers to assist with precise intraoperative and postoperative imaging.Various lordotic angles (e.g., 0°, 5°, 7°, 9°) to help restore the natural curvature of the cervical spine.Self-distracting design for ease of insertion and minimal disruption to surrounding tissues.Integration with anterior cervical plating systems for additional stability.Intended Use:
Used in cervical spinal fusion procedures to provide stability and support to the cervical spine.Commonly indicated for conditions such as degenerative disc disease, cervical spondylosis, trauma, and recurrent disc herniation.Sterilization:
Supplied sterile or non-sterile, depending on the manufacturer’s specifications.If provided non-sterile, it can be sterilized using standard autoclave methods.Compatibility:
Compatible with various anterior cervical plating systems for additional fixation and stability.Regulatory Compliance:
Must adhere to international standards such as ISO 13485 for medical devices.Compliance with specific regional regulations like FDA approval (for the USA) or CE marking (for Europe).

Polyaxial Pedicle Screw With Inner Nut Four Thread Titanium4.FI502.25 4.5 X 25mm4.FI502.26 4.5 X 30mm4.FI502.27 4.5 X 35mm4.FI502.28 4.5 X 40mm4.FI502.29 4.5 X 45mm4.FI502.30 5.5 X 30mm4.FI502.31 5.5 X 35mm4.FI502.32 5.5 X 40mm4.FI502.33 5.5 X 45mm4.FI502.34 5.5 X 50mm4.FI502.35 6.5 X 30mm4.FI502.36 6.5 X 35mm4.FI502.37 6.5 X 40mm4.FI502.38 6.5 X 45mm4.FI502.39 6.5 X 50mm

Here are the general specifications for an Orthopedic Polyaxial Pedicle Screw with Inner Nut and Four Thread made from Titanium:
Polyaxial Pedicle Screw with Inner Nut Four Thread TitaniumMaterial:
Titanium (often Ti6Al4V): Provides high strength, excellent biocompatibility, and resistance to corrosion.Design Features:
Polyaxial Design: Allows the screw head to be adjusted in multiple directions to optimize alignment and fixation.Inner Nut: Used to lock the screw head in the desired position and secure it against the rod or other fixation devices.Four Thread Configuration: Includes four threads on the screw shaft, which can enhance stability and grip within the pedicle. This might be configured as:Primary Thread: Provides secure engagement with the bone.Secondary Threads: Fine or differently pitched threads designed to improve grip and adjustability.Head Design: Typically has a slot or attachment point for connecting to spinal rods or plates.Diameter Options:
Common diameters range from 4.5mm to 6.5mm, but specific sizes may vary based on the manufacturer.Length Options:
Available in various lengths, generally from 30mm to 60mm or more, depending on the anatomical requirements and patient needs.Indications:
Spinal fixation and stabilizationTreatment of spinal deformities, fractures, or instabilityUsed in conjunction with rods, plates, and other spinal implants to achieve comprehensive spinal stabilization.Sterilization:
Supplied sterile or non-sterileCan be sterilized using standard hospital protocols (e.g., autoclaving)Compliance:
Conforms to international standards for spinal implants, such as ISO 13485 for medical devices.Additional Components:
Locking nutsSpinal rods or plates (for complete spinal fixation systems)Instrumentation for insertion and adjustment

Polyaxial Pedicle Screw With Inner Nut Single Thread Titanium4.SI502.25 4.5 X 25mm4.SI502.26 4.5 X 30mm4.SI502.27 4.5 X 35mm4.SI502.28 4.5 X 40mm4.SI502.29 4.5 X 45mm4.SI502.30 5.5 X 30mm4.SI502.31 5.5 X 35mm4.SI502.32 5.5 X 40mm4.SI502.33 5.5 X 45mm4.SI502.34 5.5 X 50mm4.SI502.35 6.5 X 30mm4.SI502.36 6.5 X 35mm4.SI502.37 6.5 X 40mm4.SI502.38 6.5 X 45mm4.SI502.39 6.5 X 50mm
Here are the general specifications for an Orthopedic Polyaxial Pedicle Screw with Inner Nut and Single Thread made from Titanium:
Polyaxial Pedicle Screw with Inner Nut Single Thread TitaniumMaterial:
Titanium (often Ti6Al4V): Alloyed for enhanced strength, biocompatibility, and corrosion resistance.Design Features:
Polyaxial Design: Allows for multi-directional angling of the screw head, providing greater flexibility in alignment and fixation.Inner Nut: Used to secure the screw in the desired position and to lock the screw head to the rod or other fixation device.Single Thread: Features a single thread configuration along the screw shaft for secure fixation within the pedicle.Threaded Shaft: Designed for optimal fixation and stability in the bone.Head Design: Usually includes a slot or attachment point to connect with spinal rods or plates.Diameter Options:
Common diameters range from 4.5mm to 6.5mm, but specific sizes may vary based on the manufacturer.Length Options:
Varies based on anatomical needs and patient specifications, typically ranging from 30mm to 60mm or more.Indications:
Spinal fixation and stabilizationTreatment of spinal deformities, fractures, or instabilityUsed in conjunction with rods, plates, and other spinal implants for comprehensive fixation.Sterilization:
Supplied sterile or non-sterileCan be sterilized using standard hospital protocols (autoclaving)Compliance:
Conforms to international standards for spinal implants (e.g., ISO 13485 for medical devices)Additional Components:
Locking nutsSpinal rods or plates (for complete spinal fixation systems)Instrumentation for insertion and adjustment

Expert Tibia Nail Titanium816T.001 8 x 240mm816T.002 8 x 260mm816T.003 8 x 280mm816T.004 8 x 300mm816T.005 8 x 320mm816T.006 8 x 340mm816T.007 8 x 360mm816T.008 8 x 380mm816T.009 9 x 240mm816T.010 9 x 260mm816T.011 9 x 290mm816T.012 9 x 300mm816T.013 9 x 320mm816T.014 9 x 340mm816T.015 9 x 360mm816T.016 9 x 390mm816T.017 10 x 240mm816T.018 10 x 260mm816T.019 10 x 2100mm816T.020 10 x 300mm816T.021 10 x 320mm816T.022 10 x 340mm816T.023 10 x 360mm816T.024 10 x 3100mmOrthopedic Expert Femur Nail Titanium SpecificationsMaterial:
Titanium alloy (commonly Ti-6Al-4V)Dimensions:
Length: Typically ranges from 300mm to 480mm, in increments of 20mmDiameter: Available in various diameters, commonly 9mm, 10mm, 11mm, 12mm, and 13mmDesign Features:
Proximal and Distal Locking: Multiple locking options to ensure stable fixation.Cannulated Design: Allows for guided insertion over a guide wire, improving surgical accuracy.Anatomical Curvature: Designed to match the natural shape of the femur, promoting proper alignment.Dynamic and Static Locking Modes: Offers both options to address different types of fractures and promote bone healing.Polished Surface: Reduces friction and irritation to surrounding tissues, promoting patient comfort.Radiolucent Properties: Titanium is radiolucent, making post-operative imaging easier and more accurate.Mechanical Properties:
High strength-to-weight ratio, providing robust support with less material bulk.Excellent biocompatibility, reducing the risk of adverse tissue reactions.Corrosion-resistant due to the titanium alloy, ensuring long-term durability within the body.Indications:
Used for the treatment of femoral fractures, including:Diaphyseal fracturesSubtrochanteric fracturesProximal and distal metaphyseal fracturesSegmental fracturesComminuted fracturesSurgical Technique:
Inserted intramedullary into the femur bone, typically under fluoroscopic guidance.Proximal and distal locking screws secure the nail, ensuring stable fixation.Designed to allow both antegrade and retrograde insertion techniques depending on the fracture location and surgical approach.Sterilization:
Supplied sterile, ready for immediate use in surgical settings.Can be sterilized using standard hospital autoclaving procedures if necessary.Regulatory Compliance:
Manufactured in compliance with ISO 13485:2016 standards for medical devices.CE marked, indicating conformity with European health, safety, and environmental protection standards.Accessories and Instruments:
Guide Wire: Facilitates the accurate placement of the femur nail.Insertion Handle: Ensures controlled insertion and positioning of the nail.Locking Screws: Available in various lengths to match the specific requirements of the fracture and patient anatomy.Targeting Device: Assists in the accurate placement of distal locking screws.Benefits of Titanium over Stainless Steel:
Lighter Weight: Titanium implants are lighter, which can be beneficial for patient comfort.Better Biocompatibility: Titanium has a lower risk of causing allergic reactions and is more compatible with human tissues.Greater Fatigue Resistance: Titanium can withstand repetitive stress better, which is advantageous for active patients.

The Orthopedic 120° Angled Blade Plate DCP (Dynamic Compression Plate) made from SS316L (Stainless Steel 316L) is a specialized implant used for treating fractures involving complex bone angles, typically in the proximal femur or tibia. It is designed to provide stable fixation in these challenging areas while promoting bone healing.
Key Features:Material:
SS316L (Stainless Steel 316L): A medical-grade stainless steel known for its high corrosion resistance, strength, and biocompatibility, making it ideal for surgical implants.Angle:
120° Angled Blade: This fixed angle allows for precise anatomical alignment and stabilization, particularly useful in fractures of the proximal femur or other areas with complex angular requirements.Blade Design:
The blade is inserted into the bone and serves to anchor the plate, providing additional mechanical stability to prevent rotation or shifting of bone fragments.Dynamic Compression Plate (DCP):
The DCP design promotes dynamic compression at the fracture site. This aids in bringing bone fragments together, enhancing healing by allowing micromotion that stimulates bone growth.Screw Holes:
The plate features several screw holes that accommodate locking or non-locking screws, providing versatile fixation options. The exact number of holes may vary based on the plate design and length.Sizes:
Available in various blade lengths and overall plate lengths to suit different patient anatomies and fracture patterns.Common Applications:Fracture Fixation: Primarily used for treating fractures in areas with a specific anatomical angle requirement, such as the proximal femur (femoral neck fractures) or tibia.Complex Fractures: Useful in cases where conventional plates cannot provide the necessary angular support.Osteotomies: Sometimes used in procedures where realignment of the bone is required through cutting and repositioning.Benefits:Precise Anatomical Fit: The 120° blade angle is designed to match the natural contour of certain bones, ensuring better alignment and stability in fracture fixation.Dynamic Compression: The DCP design applies compressive forces to the fracture, aiding in faster and more reliable bone healing.Strength and Durability: Made from SS316L, the plate is durable, corrosion-resistant, and capable of withstanding the mechanical demands of bone healing.Would you like detailed specifications for a specific model or further information on compatible screw sizes and lengths?

2.7mm DCP Plate Titanium4132.11212 Holes4132.11223 Holes4132.11234 Holes4132.11245 Holes4132.11256 Holes4132.11267 Holes4132.11278 Holes4132.11289 Holes4132.112910 Holes4132.113012 HolesThe Orthopedic 2.7mm Dynamic Compression Plate (DCP) Titanium Surgical Implant is designed for the fixation of bone fractures, particularly in smaller bones or complex fracture sites. Its titanium construction and dynamic compression capabilities make it a valuable tool for precise and effective fracture management.Material:Titanium Alloy (Ti-6Al-4V or Ti-6Al-7Nb): Titanium is chosen for its excellent strength-to-weight ratio, outstanding biocompatibility, and resistance to corrosion. It is lightweight yet strong, making it suitable for implants that need to integrate well with bone tissue.Dimensions:Plate Thickness: 2.7mm.Plate Width: Typically around 10mm to 12mm, though specific dimensions may vary based on the design and manufacturer.Length: Available in various lengths to meet different surgical needs and anatomical requirements.Design Features:Dynamic Compression Design: The DCP design incorporates oblong holes that allow for dynamic compression across the fracture site. By positioning screws in these oblong holes, the plate can compress the fracture, aiding in alignment and promoting healing.Hole Diameter: Designed to accommodate 2.7mm screws, which secure the plate to the bone.Number of Holes: The number of holes in the plate depends on its length and design, allowing for flexible screw placement and optimal fixation.Uniform Hole Spacing: Ensures even distribution of mechanical forces, reducing stress concentrations and enhancing stability.Low-Profile Design: Minimizes irritation to surrounding soft tissues and reduces the risk of postoperative complications.Application:Indications: Ideal for the fixation of small bone fractures or osteotomies, particularly in the extremities (hands, feet, and small long bones) or in complex fracture sites where precise stabilization is necessary.Surgical Use: Employed in procedures that benefit from dynamic compression to enhance fracture healing. The plate provides effective stabilization by applying compressive forces that aid in aligning and supporting the fracture.Advantages:Biocompatibility: Titanium’s excellent biocompatibility reduces the risk of allergic reactions and ensures better integration with bone tissue.Strength and Lightweight: Titanium offers a high strength-to-weight ratio, making it strong yet lightweight—ideal for delicate or confined spaces.Corrosion Resistance: Titanium’s resistance to corrosion ensures long-term durability and effectiveness of the implant.Dynamic Compression: The DCP design allows for effective compression across the fracture site, improving alignment and healing.Anatomical Fit: The plate’s design conforms to the bone structure, providing effective support and reducing the risk of implant migration or loosening.Low-Profile Design: Minimizes soft tissue irritation and postoperative discomfort, contributing to better patient outcomes.Surgical Benefits:Enhanced Stability: The dynamic compression feature of the plate offers robust support for fractures, promoting better alignment and stabilization.Reduced Complications: The biocompatibility and corrosion resistance of titanium minimize the risk of complications, including allergic reactions and implant failure.Customizable Fit: With various lengths and hole configurations available, surgeons can choose the most appropriate plate for each specific case, optimizing fixation and promoting effective healing.

ECO Mesh Cage Round Hole Titanium4.SI596.8 8mm X 100mm4.SI596.9 9mm X 100mm4.SI596.10 10mm X 100mm4.SI596.11 11mm X 100mm4.SI596.12 12mm X 100mm4.SI596.13 13mm X 100mm4.SI596.15 15mm X 100mm4.SI596.16 16mm X 100mm4.SI596.18 18mm X 100mm

Here are the general specifications for an Orthopedic ECO Mesh Cage with round holes, made from Titanium, used in spine implants:
Orthopedic ECO Mesh Cage Round Hole Titanium Spine ImplantMaterial:
Titanium (often Ti6Al4V): Provides high strength, biocompatibility, and resistance to corrosion.Design Features:
Mesh Structure: The cage features a mesh design with round holes, which allows for enhanced bone ingrowth and promotes spinal fusion by providing a scaffold for new bone formation.ECO Design: Refers to a design focused on ecological and functional benefits, potentially including optimized material use and improved biological compatibility.Shape and Configuration: May vary in shape, including cylindrical, rectangular, or other configurations to fit different intervertebral spaces and anatomical requirements.Round Holes: Designed to facilitate the penetration of bone graft material and to promote better integration with the surrounding bone.Diameter and Dimensions:
Diameter/Size: Varies based on the design and patient needs, typically ranging from 10mm to 20mm or more, depending on the intervertebral space.Length: Available in various lengths to accommodate different spinal segments, generally ranging from 20mm to 50mm or more.Indications:
Spinal fusion and stabilizationTreatment of degenerative disc disease, spinal fractures, or deformitiesProvides structural support while allowing for natural bone growth through the mesh structureSterilization:
Supplied either sterile or non-sterileCan be sterilized using standard hospital protocols (e.g., autoclaving)Compliance:
Conforms to international standards for spinal implants, such as ISO 13485 for medical devices.Additional Components:
Instrumentation: May include tools for insertion and positioning of the mesh cage.Bone Grafting Material: The mesh design allows for the incorporation of bone graft or biologics to promote fusion.