Synoviq Medical Technology (China) Co., Ltd. stands as a premier globally-oriented designer and manufacturer of state-of-the-art orthopedic implants and surgical instruments. Since our inception on March 18, 2016, we have established our identity around relentless technological innovation, uncompromising quality control, and streamlined OEM/ODM supply chains tailored to medical device distributors, multinational healthcare organizations, and specialized hospital groups worldwide.
With an extensive infrastructure occupying over 18,600 m² of advanced manufacturing floor, we optimize high-precision operations for trauma fixation systems, spinal implants, intramedullary nails, external fixations, and most critically, clinical-grade Cancellous Screws. Leveraging a robust mechanical engineering R&D team of 76 dedicated engineers, we have introduced 186 new product designs in the past calendar year alone, driving forward the frontier of implant biocompatibility, biomechanical load transfer, and surgical deployment ease.
| Metric Component | Details & Capabilities |
|---|---|
| Registered Legal Entity | Synoviq Medical Technology (China) Co., Ltd. (Brand: Synoviq) |
| Core Competency | OEM & ODM Custom Design, Prototype Development, Swiss-Type Machining, and Surface Treatment |
| Material Integrity | ISO 5832-3 Titanium Alloy (Ti-6Al-4V ELI), Implant Grade 316L Stainless Steel, PEEK |
| Quality Inspection Protocols | 100% Incoming Raw Material Analysis & 100% Final Non-Destructive Product Auditing |
| Inspection Apparatus | CMM (Coordinate Measuring Machines), Mechanical Testers, Hardness Testers, Spectrometers, Sterility Validation systems |
| Global Compliance Footprint | Class III Certifications, ISO 13485 Quality Management, CE, Cleanroom Class 100,000 |
Cancellous screws are highly specialized orthopedic fasteners engineered to optimize purchase and pullout strength in porous, trabecular (spongy) bone. Unlike cortical screws which feature shallow threads designed for dense bone, cancellous screws incorporate deep, wide-pitch threads and a larger outer-to-core diameter ratio. This geometry increases the surface area of contact, distributing shear stresses evenly across the fragile trabecular networks.
We engineer cancellous screws with wide pitches (typically 1.75mm to 3.0mm) to allow bone graft or native trabecular structures to pack between threads, vastly improving axial pull-out resistance.
Our Swiss-lathe processing allows us to produce micro-cannulations down to 1.1mm inner diameters. Guiding wires can be fed directly through the screw, enabling minimally invasive surgical placement.
We deploy Type II Type III titanium anodization. This creates an inert, biologically passive titanium oxide layer, reducing friction, eliminating cold welding, and allowing color-coded sizes.
For orthopedic brands looking for OEM and ODM manufacturing partnerships, Synoviq offers highly adaptable design paths. Whether modifying the head profile (e.g., low-profile, countersunk, or headless compression style) or adjusting the self-tapping flute density to eliminate the need for tapping tools during emergency trauma surgeries, our design team translates raw clinical concepts into physical titanium products.
Producing orthopedic implants demands absolute conformity to dimensional tolerances and chemical compositions. Below is our internal technological pipeline, visually detailing the machining, design, verification, and testing methodologies that safeguard our product integrity.























Bone density, clinical regulatory environments, and surgical access methods vary by region. We accommodate these local trends to ensure our cancellous screws deliver optimal therapeutic results:
Emphasis on ASCs (Ambulatory Surgery Centers) requires single-use, sterile-packed implants. Our leakage and packaging validation systems assure high sterile barrier shelf life up to 5 years, facilitating direct-to-OR logistics.
The transitions to EU MDR demand full traceabilities and mechanical validation reports. Synoviq provides comprehensive ISO 5832-3 mill test certifications and ASTM F543 torque/axial pull-out data files for CE regulatory submission.
A high incidence of fragility fractures requires cost-efficient, high-performance implants. We manufacture cannulated compression screws with customizable thread depths to optimize purchase in lower-density osteoporotic bone.
In the global medical device sector, manufacturing resilience relies heavily on raw material access, processing technology, and fast shipping logistics. Operating from the heart of China’s advanced medical hardware corridor allows Synoviq to secure major structural benefits for our international buyers:
We source high-purity medical-grade titanium directly from state-approved alloy foundries, ensuring zero micro-fractures, stable mechanical properties, and consistent biocompatibility.
With an in-house team of 76 R&D design engineers, we can translate complex custom screw specifications into CAD/CAM models within 48 hours and deliver sample prototypes in under 15 days.
Located close to major international shipping hubs, we reduce sea and air transit times to Europe, North America, and Southeast Asia, supported by a network of over 1,120 supply partners.
As clinical methodologies evolve toward less invasive interventions and faster healing cycles, Synoviq continues to adapt. Our current R&D pipeline focuses on several key areas designed to improve orthopedic clinical outcomes:
Developing magnesium-alloy and high-purity PLLA/PLGA composite designs that match cancellous load distributions and dissolve as new bone forms, eliminating secondary surgeries.
Using electron beam melting (EBM) to print micro-porous, biomimetic surface layers onto titanium screws, encouraging quick osseointegration and stable long-term fixation.
Applying active silver-ion coatings and surface micro-texture patterns that disrupt bacterial cell membranes, lowering the risk of implant-associated infections.
We primarily utilize medical-grade Titanium Alloy (Ti-6Al-4V ELI conforming to ISO 5832-3 and ASTM F136 specifications) and high-quality 316L Stainless Steel. These materials provide high fatigue strength, excellent biocompatibility, and optimal elastic moduli compatible with bone.
Yes. As a dedicated OEM/ODM manufacturer, we can customize parameters such as pitch depth, thread type (fully or partially threaded), drive style (e.g., torx, hex, cruciform), and self-tapping/self-drilling flutes to meet your surgical specifications.
We run a 100% final inspection process. Our testing laboratory performs metallographic analysis, chemical spectrometer verification, CMM dimensional checks, hardness profiling, and mechanical axial pull-out and torsional testing to ensure compliance with international standards.
Yes. We operate a Class 100,000 cleanroom cleaning, assembly, and packaging line. Implants can be supplied in sterile blister packaging, validated through our steam sterilization and leakage testing systems, ready for surgical use.
We support our partners with comprehensive documentation, including material traceabilities, ISO 13485 quality credentials, biocompatibility profiles, and CE/FDA filing dossier support to facilitate regulatory registration.
Standard product orders are typically manufactured and dispatched within 30 to 45 days. For highly customized OEM/ODM projects requiring tooling modifications, lead times range from 45 to 60 days, depending on technical complexity.
We use hard-anodization techniques (Type II and Type III) on our titanium screws. This process creates an oxide surface layer that reduces friction and prevents micro-galling or cold welding when used with locking plates.
Our standard catalog ranges from micro-fixation screws (2.0mm and 2.4mm outer diameters) for hand and foot surgeries, up to large fragment screws (6.5mm and 7.3mm outer diameters) designed for hip and pelvic fractures.