The Cervical Spinal Fixation (CFS) System represents the forefront of posterior stabilization, meticulously developed to address severe segment instability in the cervical and upper thoracic regions. Engineered with bio-compatible titanium alloys (Ti-6Al-4V ELI), our implants focus on stabilizing and facilitating fusion across the complex occipito-cervico-thoracic junction.
Our systems mitigate stress-shielding, a common failure point in conventional posterior systems, by optimizing load-sharing dynamics between the implant and host bone. Precision-manufactured polyaxial cervical screws offer up to 40 degrees of multi-planar angulation, simplifying alignment and insertion in complex anatomical corridors without sacrificing mechanical pull-out strength.
Strict quality-controlled spinal implants manufactured to meet stringent medical safety profiles and certified for high-risk surgical applications.
Grade 5 medical-grade titanium alloy minimizes mechanical stiffness mismatch, promoting natural bone healing processes and fusion pathway support.
The Fule COX 6.0 series features expansion zones, securing screws in osteoporotic bone beds and reducing post-operative loosening rates.
As a premier Chinese orthopedics manufacturer established in 1996, we combine 30 years of medical machining expertise with advanced testing labs to produce high-precision spinal fixation systems.
ISO13485 (04724Q10000818) Approved
In the global spinal medical device market, orthopedic surgeons and distributors struggle with rising implant costs and supply reliability issues. Global importers need consistent manufacturing capacity that does not compromise patient safety or clinical success.
We solve this with a vertical integration strategy. By sourcing raw medical titanium from qualified suppliers and handling all finishing, anodization, and testing in-house, we control costs and guarantee batch consistency. Our 30-year track record ensures a stable supply chain, helping distributors maintain consistent inventory levels.
An inside look at our certified production floor, CNC precision machining rooms, product testing labs, cleanroom assembly lines, and raw material storage areas.
We use Class III implantable titanium alloy (Ti-6Al-4V ELI) conforming to ASTM F136 specifications. This medical-grade material provides the optimal combination of high fatigue strength, corrosion resistance, and biocompatibility, minimizing long-term tissue reactivity.
Our COX 6.0 expandable system utilizes a novel expansion design. Once the screw is inserted, internal expansion mechanics deploy to lock into the bone bed. This increases radial contact area and increases pull-out resistance, helping prevent screw loosening in compromised bone.
Under ISO 13485 standards, we inspect 100% of our products. Our 15 QA/QC inspectors oversee raw material spectrometry, coordinate measuring machine (CMM) dimensional checks, surface finish profiling, dynamic mechanical fatigue testing, and cleanroom bioburden audits.
Yes. We offer sample processing, graphic adjustments, custom markings, and specialized container design to meet the regulatory and branding needs of our global distribution partners.
These systems are indicated for stabilization procedures in patients with degenerative disc disease, spinal stenosis, trauma, fracture, dislocation, spinal deformities (such as scoliosis or kyphosis), tumor-induced instability, or failed previous fusions.
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