Explore our flagship portfolio of CE-certified orthopedic implants, surgical instruments, and trauma fixation assemblies, designed in synergy with our patellar arthroplasty platforms.
| Operational Parameter | Manufacturing & Engineering Specifications |
|---|---|
| Company Entity | Synoviq Medical Technology (China) Co., Ltd. |
| Manufacturing Footprint | 18,600 m² ISO-certified clean production facility |
| Core Capabilities | CNC Milling, Swiss-type Turning, Vacuum Sintering, Precision Polishing, Cleanroom Packaging |
| R&D Team Size | 76 Engineers specialized in biomechanics and material science |
| Quality Control Staff | 48 dedicated QC inspectors conducting 100% final inspections |
| Annual Export Volume | USD 21.8 Million |
| Testing Instrumentation | CMM Measurement, Tensile Testers, Surface Roughness Testers, Spectrometers, Hardness Testers, Sterility Validation |
| Regulatory Alignments | ISO 13485:2016 Quality Management, CE Certification, FDA Compliant Operations |
| Material Selections | Titanium Alloy (Ti-6Al-4V ELI), UHMWPE (GUR 1020/1050), Ceramic Composite, PEEK |
Synoviq maintains strict quality control at every phase of production. From raw material inspection using optical spectrometers to Swiss-type CNC machining and multi-axis automated polishing, every component is manufactured in controlled environments. Our physical testing laboratories feature coordinate measuring machines (CMM), tensile testers, and digital microscopes to verify dimensional accuracy and structural integrity.
Here are key technical answers regarding material quality, manufacturing tolerances, and compliance standards for patellar component procurement:
We use high-purity medical-grade UHMWPE (specifically GUR 1020 and GUR 1050) conforming to ASTM F648 and ISO 5834-2. For metal-backed designs, we utilize Ti-6Al-4V ELI titanium alloy matching ASTM F136 specifications to ensure biocompatibility and fatigue resistance.
Implant configurations undergo wear simulation testing under ISO 14243 standards, exposing the components to millions of cycles of physiological loading. Joint wear and surface changes are assessed using coordinate measuring machines and gravimetric methods.
Most products are sterilized using Ethylene Oxide (EtO) validation or Gamma Irradiation (Co-60) in compliance with ISO 11135 and ISO 11137. We also supply components in non-sterile bulk packaging for partners who run their own packaging and sterilization programs.
We manufacture both cemented patellar components, featuring PMMA-receptive undercut fixation pegs, and cementless models, which use porous titanium coatings or sintered metal structures to encourage osseointegration.
Yes. Our engineering team uses 3D modeling and FEA tools to develop custom implant profiles, peg layouts, and dimensions based on partner specifications.
Discover our range of surgical saws, specialized retractors, and osteotomy tools designed to assist in precision joint reconstruction and orthopaedic trauma care.