OEM/ODM Interference Screws For ACL Manufacturer & Exporters

Precision Sports Medicine Engineering: High-Performance Biomaterials, Advanced Cannulation, and Tailored Fixation Solutions for Global Knee Reconstruction Brands

GLOBAL ORTHOPEDIC MANUFACTURING EXCELLENCE

Moventra Medical Technology (China) Co., Ltd.

Established in 2017, Moventra Medical Technology (China) Co., Ltd. is a preeminent developer and manufacturer specializing in sports medicine implants, trauma, spine, joint reconstruction, and precision orthopedic instrument sets. Spanning an advanced 18,600 m² class-leading manufacturing center, Moventra leverages Swiss-type CNC machining, multi-axis milling, and intelligent quality verification protocols to deliver exceptional medical device products to customers worldwide.

Our Sports Medicine line—particularly our state-of-the-art ACL/PCL Interference Screws—represents the pinnacle of mechanical and biological co-design. Utilizing premium grade bioabsorbable polymers and implants-grade PEEK, we engineer fixation systems that resolve the primary challenges of soft-tissue and bone-tendon-bone (BTB) reconstruction. By providing robust primary stability, minimizing tissue shear stress, and offering precise cannulated configurations, Moventra implants support rapid osteointegration and reliable clinical outcomes.

18,600m²
Modern CNC Facility
$23.8M
Annual Export Revenue
86
R&D Engineers
100%
Pre-Shipment Quality Check
Strategic Core Specification Manufacturing & Operational Capability Details
Company Name & Brand Moventra Medical Technology (China) Co., Ltd. | Brand: Moventra
Established & Experience Founded in 2017; 13 years of industry-deep experience and 7 years of global export compliance.
R&D Capability & Output 86 R&D engineers, releasing 156 new clinical-grade products annually. Independent CAD/CAM modeling, finite element analysis (FEA), and rapid metal/polymer prototyping.
Supply Chain Scale Over 1,120 global supply chain partners, ensuring highly resilient sourcing of medical grade PEEK, Titanium (Ti-6Al-4V ELI), and Bioabsorbables.
Customization Scope (OEM/ODM) Advanced drawing/sample-based contract manufacturing, custom pitch/thread profiling, laser branding, and bespoke packaging configurations (sterile blister pack/sterile tube).
Quality Control Force 48 full-time QA/QC inspectors, conducting 100% dimensional inspection, material spectrometry, surface finish profiles, mechanical torque limit validation, and sterile packaging integrity tests.
Primary Target Markets North America, Europe, South America, Middle East, Southeast Asia, Australia.
Interference Screws for ACL: Advanced Mechanical & Biological Design
Optimized thread profiles, customized materials, and robust insertion characteristics engineered for outstanding surgical performance.

Material Options: PEEK, Titanium, & Bioabsorbable Polymers

We supply interference screws crafted from biocompatible materials. Our PEEK (Polyetheretherketone) screws offer mechanical properties close to natural cortical bone, providing excellent radiolucency with zero artifacts during MRI/CT scans. For high-torque demands, Grade 5 Titanium (Ti-6Al-4V ELI) ensures maximal pull-out strength. Additionally, our bioabsorbable variants (PLDLA/TCP formulations) gradually transfer mechanical load to the regenerating native bone tissue.

Optimized Thread Pitch & Cannulation

Moventra's screws feature a smooth, rounded thread design specifically engineered to prevent graft laceration during insertion. Our cannulated configurations support precise guide wire positioning. The variable thread pitch provides excellent purchase in both dense cancellous bone and soft tissue grafts, delivering immediate mechanical stability and preventing post-operative micromotion.

High Torsional Limit & Driver Engagement

Designed with star-drive or hexalobe drive interfaces, our interference screws maximize driver contact area. This reduces the risk of head strip or driver slip during high-torque insertions. Every manufacturing batch undergoes rotational torque-to-failure testing to guarantee safe intraoperative application under real-world surgical pressures.

Information Gain: Clinical Fixation Dynamics in Sports Medicine

Traditional interference screws often fail due to three mechanical flaws: graft slippage under cyclic loading, mechanical mismatching causing local bone resorption, and driver socket striping. Moventra addresses these failure modes by engineering the implant thread profile using Finite Element Analysis (FEA) to distribute forces evenly. Our PEEK-OPTIMA™ grade screws exhibit a modulus of elasticity of 3.6 GPa, preventing stress shielding, while our custom star-drive geometry supports up to 4.2 Nm of torque without degradation.

Modulus of Elasticity 3.6 GPa (PEEK-OPTIMA™ matched to bone dynamics)
Torque-to-Failure Limit Exceeds 4.2 Nm (Clinical requirement: 2.5 Nm)
Thread Profile Geometry Patented dual-lead, non-lacerating round-edge thread
Guide Wire Cannulation Ø1.1mm to Ø2.0mm precise internal clearance
Precision Manufacturing Center: China Factory 4.0
Our 18,600 m² state-of-the-art facility integrates Swiss-type CNC machining and comprehensive inspection systems for orthopedics.
Swiss-type CNC
Swiss-type Machining
Lathe and Milling
Lathe and Milling
Machining
Machining Center
Testing
Mechanical Testing
Assembling
Cleanroom Assembly
Warehouse
Logistics Warehouse
Swiss-type lathe
Swiss-type lathe
Lathe and milling machine
Lathe and milling machine
Lathe
Precision Lathe
Machining center
Machining center
Wire cutting machine
Wire cutting machine
Grinding machine
Grinding machine
Three-coordinate measuring machine
Three-coordinate measuring
Two-dimensional micrometer
Two-dimensional micrometer
Hardness tester
Hardness tester
Microscope
Microscope Inspection
Global Procurement, Localization & Regulatory Compliance
How Moventra satisfies international quality standards, local regulations, and resilient supply chain objectives.

Global Regulatory Certifications

Navigating MDR (Medical Device Regulation) in Europe and FDA pathways in the USA requires traceabilty. Moventra maintains ISO 13485 quality systems, delivering full biocompatibility verification (ISO 10993) and comprehensive trace documentation (material certificates, dimensional reports, sterilization validation) for seamless global registration.

Resilient Supply Chains for Medical Brands

Unpredictable lead times damage brand relationships. With 1,120 reliable supply chain partners and extensive material inventory buffers, Moventra buffers global partners against shortages. Our dual-source titanium and PEEK access models keep lead times consistent even during peak demand periods.

Localized Customization & Engineering

Different markets have distinct anatomical preferences and surgeon habits. Moventra offers flexible localized support, including customizable sizing (screws from Ø5mm to Ø11mm with lengths up to 35mm), specialized thread styling, and localized sterile blister packing in compliance with local health department mandates.

Sports Medicine Technology Roadmap & Future Outlook
Investing in the next generation of bioactive interfaces, porous polymer constructs, and smart surgical instrumentation.

Porous PEEK (Carbon-Fiber Reinforced)

To reduce stiffness discrepancies and promote direct bony ingrowth, Moventra's R&D is developing porous PEEK structures. By integrating localized micro-porosity at the screw threads, we mimic natural cancellous bone, encouraging cellular attachment and improving long-term pull-out resistance.

Magnesium-Based Biodegradable Alloys

Moving beyond traditional PLA/PLDLA polymers, Moventra is investigating magnesium-based biodegradable metals. These alloys provide the mechanical strength of titanium during the initial critical healing phase, followed by controlled degradation into natural, non-toxic magnesium ions that support new bone formation.

Bioactive Surface Coatings

Enhancing osteoconduction at the bone-screw interface is essential. We are testing biomimetic coatings, including Hydroxyapatite (HA) and Calcium Phosphate (CaP) electro-deposition, to accelerate initial bone bonding and minimize the fibrous capsule formation occasionally associated with inert polymer implants.

Clinical & Commercial FAQ
Answers to technical and regulatory questions for global medical brand procurement managers.
What grades of PEEK and Titanium does Moventra use for interference screws?
We manufacture exclusively with implant-grade materials. Our PEEK screws are machined using premium PEEK-OPTIMA™ or high-grade medical equivalents that satisfy ISO 10993 biocompatibility requirements. Our metallic implants use Grade 5 Titanium (Ti-6Al-4V ELI) satisfying ASTM F136 specifications, which ensures high mechanical strength and fatigue resistance.
What torque values can your PEEK interference screws safely withstand?
Our cannulated PEEK interference screws are engineered to withstand torsional loads exceeding 4.2 Nm without head deformation. This is well above typical intraoperative insertion torques, which range between 1.5 to 2.5 Nm, providing a wide safety margin during challenging ACL graft fixations.
What OEM/ODM customization options are available for sports medicine implants?
We offer comprehensive customization, including changes to thread pitch, variable-taper profiles, star/hexalobe drive dimensions, custom laser engraving for branding, and sterile packaging options. We can manufacture directly from customer CAD drawings or reverse-engineer from physical samples.
How does Moventra ensure 100% quality inspection for medical implants?
Every production lot undergoes rigorous multi-step inspection: material certification via spectrometer analysis, automated coordinate measuring machine (CMM) testing to verify thread tolerance, surface roughness profiling, destructive torque-to-failure batch testing, and final cleanroom particle and sterility audits prior to packaging.
Are your manufacturing processes compliant with CE MDR and FDA guidelines?
Yes, Moventra is certified under ISO 13485. Our manufacturing workflows, cleanroom assembly systems, and testing laboratories align with international standards. We supply our OEM partners with the comprehensive technical documentation and trace files required for local CE MDR and FDA registrations.