Premium surgical components manufactured under rigorous medical-grade standards, ensuring stability and clinical efficacy.
Unlocking superior biomechanical outcomes with advanced cortical button design and material integration.
Anterior Cruciate Ligament (ACL) reconstruction requires absolute surgical precision and biomechanically superior fixation components. The mechanical environment of the knee demands implants capable of resisting cycle loading patterns under daily human movement. As suspensory cortical fixation has emerged as the gold standard for femoral graft placement, ACL reconstruction buttons must provide exceptional pull-out strength, minimal displacement, and simple deployment properties.
Our research and clinical feedback emphasize the transition from traditional titanium alloy fixed-loop buttons to adjustable-loop configurations, enhancing initial graft tension and simplifying intraoperative adjustment.
By using medical-grade Titanium Alloy (Ti-6Al-4V ELI) and high-density polymers like PEEK (Polyetheretherketone), modern manufacturers can produce devices that eliminate the "bungee-effect" and prevent tunnel widening, optimizing graft integration and patient recovery times.
We source raw medical-grade Titanium and ultra-high-molecular-weight polyethylene (UHMWPE) fiber material directly from certified global distributors. This ensures that every manufactured loop and button has the required microstructural purity to pass biocompatibility tests (ISO 10993) and support high-tensile loads exceeding 1200 N without structural failure.
Clinically validated to endure over 100,000 gait cycles at physiological stress levels, our buttons undergo testing on advanced axial fatigue testers, maintaining residual displacement under 1mm to minimize graft slippage post-surgery.
A professional manufacturer of orthopedic implants and surgical instruments, dedicated to delivering innovative, reliable, and high-quality medical solutions for healthcare professionals worldwide.
Synoviq Medical Technology (China) Co., Ltd. has focused on research, development, precision manufacturing, and international quality standards, providing comprehensive OEM and ODM services for global medical device brands, distributors, and hospitals since its establishment on March 18, 2016.
Our product portfolio includes trauma fixation systems, spinal implants, locking plates, intramedullary nails, external fixation systems, orthopedic screws, surgical instruments, and customized orthopedic solutions. Equipped with advanced CNC machining centers, precision inspection equipment, and modern clean production facilities, we ensure every product meets strict international quality requirements.
Driven by continuous innovation, Synoviq invests heavily in R&D and intelligent manufacturing to enhance product performance, surgical efficiency, and patient outcomes. Our experienced engineering team works closely with customers to develop customized products tailored to different clinical applications and market demands. Synoviq has established long-term partnerships with distributors, medical brands, and healthcare organizations across Europe, North America, South America, the Middle East, and Asia-Pacific.
| Item | Information |
|---|---|
| Company Name | Synoviq Medical Technology (China) Co., Ltd. |
| Brand | Synoviq |
| Established | March 18, 2016 |
| Building Area | 18,600 m² |
| Annual Export Revenue | USD 21.8 Million |
| Export Experience | 8 Years |
| Industry Experience | 14 Years |
| Quality Inspection | 100% Final Inspection & Incoming Material Inspection |
| Product Inspection Methods | CMM Measurement, Mechanical Testing, Surface Roughness Testing, Hardness Testing, Salt Spray Testing, Sterility Validation |
| Quality Control Staff | 48 |
| Business Type | Manufacturer & Exporter (OEM/ODM) |
| Main Markets | Europe, North America, South America, Middle East, Southeast Asia |
| Supply Chain Partners | 1,120+ |
| Main Customer Types | Medical Device Brands, Importers, Distributors, Hospitals, Government Procurement Projects |
| R&D Capability | Independent Product Design, Prototype Development, Clinical-Oriented Engineering, OEM & ODM Development |
| Customization Options | Logo Customization, Packaging Customization, Product Design Customization, Material Selection, Surface Treatment |
| New Products Released Last Year | 186 |
| R&D Engineers | 76 |
Production Facility
Annual Export Value
R&D Engineers
Sterility & QA Check
Every stage of production—from raw cutting to microscopic surface validation—is strictly executed in-house using class-leading machinery.
Mitigating supply chain risks, establishing regulatory alignment, and maximizing value for clinical procurement.
Procuring ACL Reconstruction buttons demands absolute precision. Major medical importers look for options that balance loop elongation control with bone-preserving footprints. Our customizable loop selections (ranging from 10mm to 60mm loops or customizable adjustable loops) provide maximum versatility during single-stage or two-stage reconstruction surgeries.
Navigating MDR (Medical Device Regulation) in Europe, CE standards, and FDA 510(k) clearances is vital for international sports medicine distributors. Synoviq assists our global partners by providing complete technical documentation, including raw material traceability records, tensile biomechanical test metrics, and ETO sterilization verification files.
Every clinical market has distinct surgical preferences regarding button shapes, loop configurations, and pre-loaded pull threads. Synoviq's dedicated 76 R&D engineers customize dimensions, modify button edge profiles to prevent suture fraying, and optimize pre-threaded configurations for easier intra-operative pull paths.
Where sports medicine meets advanced manufacturing technologies.
The next era of ACL suspensory fixation moves beyond mechanical strength toward bio-inductive integration. We are focusing on surface-treated titanium surfaces coated with thin layers of bioactive materials (such as Hydroxyapatite) to encourage local osteointegration directly at the femoral cortex interface. This reduces the micro-motion responsible for tunnel enlargement, improving clinical outcomes for patients undergoing active rehabilitation.
While titanium remains widely used, carbon-reinforced PEEK implants are gaining traction due to their radiolucent properties and elastic modulus, which is similar to cortical bone. Our production lines are being upgraded to process specialized PEEK variants, enabling the design of next-generation interference screws and fixation buttons that minimize artifacts during postoperative MRI scans.
Phase 1: Bio-absorbable Loops - Developing PLA/PLLA polymer blends designed to gradually transfer tension to the bone tunnel over a 12-month post-operative period.
Phase 2: Ultra-low Profile Designs - Minimizing femoral cortical footprint to prevent soft-tissue irritation and lateral knee pain in thin patients.
Phase 3: Digital Integration - Adding unique batch QR identifiers directly onto the button surface via high-precision laser marking for tracking throughout the device's lifecycle.
Technical answers regarding raw material certification, performance testing, and production capabilities.
Expand your product portfolio with specialized instruments and implants trusted by orthopedic surgeons globally.