Axiora Medical Axiora Medical
Next-Generation Orthopedic Implants

OEM/ODM Herbert Screws Exporter & Exporters

Precision Engineering, ISO 13485 Compliance, and Dynamic Compressive Fixation Solutions for Global Medical Device Brands and Clinical Distribution Networks.

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Surgical Principles & Compressive Biomechanics of Herbert Screws

Why Headless Compression Screws (HCS) Are Essential in Reconstructing Small-Bone Fractures.

The Herbert Screw represents a key advancement in orthopaedic trauma fixation, particularly for small bone osteosynthesis. Originally designed by Timothy Herbert, the primary mechanical innovation is the differential pitch mechanism. Unlike standard surgical screws with a uniform thread pitch, a Herbert screw incorporates a leading thread with a wider pitch and a trailing thread with a narrower pitch. As the screw crosses the fracture line and engages both proximal and distal fragments, the differential pitch causes the fragments to draw together, creating controlled internal compression without the need for a projecting screw head.

Key Biomechanical Advantage:

By eliminating a traditional screw head, the implant can be driven fully below the articular surface. This is critical for cartilage-covered structures like the scaphoid bone, radial head, and osteochondral junctions, minimizing the risk of soft tissue irritation, impingement, or joint damage during post-operative rehabilitation.

Optimizing Thread Profile and Cannulation

Modern medical design relies heavily on cannulated Herbert screws. The central cannulated channel allows orthopaedic surgeons to insert a precise guide wire (typically 0.8mm to 1.2mm in diameter) across the targeted fracture or osteotomy site under fluoroscopy. The hollow screw is then guided over the wire, ensuring accurate anatomical positioning. Axiora Medical Technology designs these threads using high-fidelity finite element analysis (FEA) to maximize pull-out strength while minimizing bone damage during insertion.

15+
Years of Industry Experience
86
R&D Engineers
18.6k m²
Modern Factory Facility
USD 26M
Annual Export Revenue

Axiora Medical Technology Corporate Portfolio

A trusted global manufacturer specializing in the research, development, and supply of orthopedic implants.

Axiora Medical Technology (China) Co., Ltd. is a professional manufacturer specializing in the research, development, production, and global supply of high-quality orthopedic implants and surgical instruments. Our product portfolio covers trauma fixation systems, spinal implants, joint reconstruction solutions, sports medicine products, and related orthopedic surgical instruments.

Established with a commitment to innovation and precision manufacturing, Axiora integrates advanced CNC machining, automated production lines, and strict quality management systems to deliver reliable products that meet international standards. Our experienced engineering team continuously develops innovative solutions to support surgeons and healthcare providers worldwide.

With strong OEM and ODM capabilities, we provide customized manufacturing services according to customers' drawings, samples, and technical requirements. From product design and prototyping to mass production and packaging, our integrated manufacturing process ensures consistent quality, competitive pricing, and on-time delivery.

Today, Axiora exports its orthopedic products to customers across Europe, North America, South America, the Middle East, Southeast Asia, and Africa, building long-term partnerships with medical device distributors, brand owners, hospitals, and healthcare organizations around the world.

Company Information Summary

Specification Category Operational details
Company Name Axiora Medical Technology (China) Co., Ltd.
Brand Name & Domain Axiora (www.axioraortho.com)
Established Year 2017 (15 Years industry experience background)
Factory Infrastructure 18,600 m² cleanroom & manufacturing floor space
Annual Export Volume USD 26 Million
Export History 8 Years of direct international shipping and registration support
Quality Inspection Protocols 100% finished product inspection & incoming material control
Product Inspection Methods Coordinate Measuring Machine (CMM), Tensile Testing, Hardness Testing, Surface Roughness Inspection, Salt Spray Testing
Quality Control Staff 48 Quality Engineers and Inspectors
Primary Business Model Manufacturer & Exporter (OEM / ODM / Private Label)
Active Global Markets Europe, North America, Middle East, Southeast Asia, South America
R&D Capability & Staff 86 Dedicated Engineers, Reverse Engineering, CAD/CAM prototyping
Customization Capabilities Laser engraving, custom packaging, drawing-based OEM, bespoke thread pitches
Innovation Index 126 new implant designs and instrumentation lines launched last year

Advanced Cleanroom Manufacturing & Quality Control Workflow

Tracing raw titanium materials through precision CNC machining, testing, and aseptic packaging.

Raw Material Inspection
Raw Material
Longitudinal Cutting
Longitudinal Cutting
CNC Machining
CNC
Polishing Stage
Polishing
Ultrasonic Washing 1
Ultrasonic Washing 1
Grinding Operations
Grinding
Sand-Blasting Treatment
Sand-Blasting
Penetrant Testing
Penetrant Testing
Anodizing Surface Treatment
Anodizing
Ultrasonic Washing 2
Ultrasonic Washing 2
OQC Final Inspection
OQC
Aseptic Packing Cleanroom
Aseptic Packing Room
Packing Line
Packing Line
Warehouse Storage
Storage
Longitudinal Cutting Lathe Machining
Longitudinal Cutting Lathe
CNC Mill-Turn Machine
CNC
Automatic Polishing Machine
Polishing Machine
Industrial Ultrasonic Washer
Ultrasonic Washing Unit
Precision Grinding Machine
Grinding Machine
Sand-blasting Cabinet
Sand-Blasting Machine
Chemical Anodizing Line
Anodizing Machine
Cleanroom Entry & Operations
Aseptic Packing Room
NDT Dye Penetrant Testing Room
Penetrant Testing Room
Fatigue and Mechanical Endurance Tester
Endurance Tester
Material Aging Tester
Aging Tester

Biocompatible Coatings & Materials

The global orthopaedic implant market is transitioning rapidly from standard titanium alloy (Ti-6Al-4V) to advanced surface-treated alloys. Type II anodization and acid-etched surfaces improve the osteointegrative capacity of small bone fasteners. Medical brands expect OEM exporters to offer these surface finishing treatments to reduce post-surgical recovery times.

ISO 13485 & MDR Compliance

Regulatory frameworks such as the European Medical Device Regulation (EU MDR 2017/745) and FDA 510(k) clearances demand total structural and material traceability. OEM/ODM exporters must provide raw material heat treatment records, ultrasonic cleaning validations, and mechanical fatigue data. Non-compliant suppliers face significant market barriers.

Minimally Invasive Guided Surgery

Surgical workflows are shifting toward minimally invasive approaches. Because of this, cannulated systems are now standard practice. Exporters must produce custom guide wires, cannulated drills, and counter-sink sleeves configured for exact integration with the Herbert screw threads. This ensures reliable surgeon tactile feedback and precise insertion.

Comprehensive B2B OEM & ODM Integration Solutions

How Axiora bridges the gap between implant concept design and sterilized hospital delivery.

Managing a global medical supply chain requires consistency and reliability. Axiora Medical Technology minimizes manufacturing variations by using a single-source setup from incoming titanium alloy analysis to sterile cleanroom packaging. Our factory has 1,120 supply chain partners, ensuring stable material acquisition and production continuity during high-volume contract demands.

1. Material Traceability & Biomechanical Performance

We source medical-grade titanium alloys (Ti-6Al-4V ELI, conforming to ASTM F136 standards) exclusively from verified, certified mills. Every batch undergoes a series of physical inspections including tensile strength validation, hardness mapping, and chemical composition spectrum analysis. This level of quality control ensures that our Herbert screws maintain structural integrity during insertion torque loads and cyclic physiological loading in bone fixation.

2. Complete Instrument & Implant Integration

A surgeon's choice of implant is heavily influenced by the ease of use of the surgical instrument set. Axiora manufactures both the implants and their dedicated instrumentation kits. This includes cannulated screwdrivers, depth gauges, drill guides, and parallel wire guides. Our matching instrument systems help ensure the screw engages properly and reduces driver slippage during surgery.

Advanced Testing & Packaging Safeguards:

To support global medical device brands, we provide complete technical documentation dossiers, including cleanroom packaging validation (ISO 11607), gamma irradiation sterilization studies, and shelf-life aging tests (ASTM F1980).

3. Global Logistics & Regulatory Support

Axiora supports distributors and importers with comprehensive customs clearance documentation, certificate of analysis (COA) generation, and registration dossier compilation (CE, ISO 13485, and country-specific filings). We maintain strict quality oversight at every stage of production to minimize shipping disruptions and help ensure compliance with regional healthcare standards.

Future Outlook: Technical Roadmap (2025–2030)

Innovative trends shaping the next generation of small-bone internal fixation devices.

As micro-surgery demands higher precision, the design of Herbert screws continues to evolve. Axiora's R&D team, comprised of 86 engineers, is actively testing two primary development pathways:

  • Absorbable Magnesium Alloys: Developing biodegradable magnesium-based headless compression screws. These implants maintain stable mechanical fixation during bone healing and gradually resorb, eliminating the need for a secondary removal surgery.
  • Robotic-Assisted Navigation Coatings: Incorporating specialized surface geometries that improve imaging contrast under real-time intraoperative 3D fluoroscopy and robotic optical systems, allowing for faster and more precise guided placement.

Technical & B2B Procurement Q&A

Technical details, ordering info, and customization questions answered by our engineering team.

What raw materials are used for your Herbert Screws, and can you provide certified analysis reports?
We use medical-grade Titanium Alloy (Ti-6Al-4V ELI) conforming to ASTM F136, as well as high-grade biocompatible 316LVM Stainless Steel (ASTM F138). Every export batch is accompanied by a mill test certificate, chemical spectrum breakdown, and physical tensile testing verification reports.
How does the differential pitch mechanism generate compression in the fracture?
The screw features a wider pitch at the leading tip and a narrower pitch at the trailing head. As the screw is driven into the bone, the leading section travels faster than the trailing section. This difference pulls the two bone fragments together, generating compression without relying on a protruding screw head.
What customization options are available for OEM/ODM clients?
We offer extensive custom options, including bespoke thread pitches, custom cannulation IDs (e.g., 0.8mm to 1.4mm), custom total lengths, laser-marked branding/logos, anodization colors, and sterile-packaged OEM boxing configurations.
Are your manufacturing processes compliant with ISO 13485 and global standards?
Yes, our manufacturing facility operates under a certified ISO 13485 quality management system. Our cleaning, passivating, and primary packaging lines are housed within Class 100,000 (ISO Class 8) cleanrooms. This ensures our implants meet bioburden and particulate requirements before sterilization.
What is the typical lead time for custom OEM batches of cannulated screws?
For standard sizes, lead times are typically 30 to 45 days. Custom OEM products requiring specialized tooling or custom thread profiles generally take 45 to 60 days. This includes drawing approval, sample confirmation, run-in tests, and full production.
How do you verify the surface roughness (Ra) of the finished screws?
Every production batch undergoes surface roughness testing using contact profilometers. For joint-adjacent implants, we maintain surface finishes within specified Ra limits (typically under 0.4 μm for polished surfaces) to prevent micro-frictional wear on surrounding tissues.
Do you supply matching instrumentation and sterilizing trays?
Yes, we provide matching instrument sets, including cannulated drills, drivers, parallel wire guides, and anodized aluminum sterilizing trays. This allows you to offer surgeons a complete implant and instrument system.
What testing procedures are used to evaluate implant fatigue limits?
We use multi-axis fatigue and endurance testers to evaluate mechanical performance. Our team performs axial pull-out force trials, torsional shear resistance tests, and cyclic bending fatigue tests. These procedures are designed to ensure our implants withstand in-vivo forces without failure.

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