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In modern small-bone osteotomy and fracture fixation, achieving high-compression, stable osteosynthesis without hardware prominence is the gold standard. Headless cannulated compression screws—popularly known through advanced designs like Acutrak Screws and traditional Herbert Screws—have revolutionized small-joint reconstruction and hand/foot trauma treatments.
By utilizing a variable pitch thread profile and a tapered core, these implants deliver continuous, dynamic compression throughout the insertion depth. As the screw moves forward, the thread pitch decreases, drawing the distal and proximal bone fragments together without the need for a traditional screw head. This avoids articular irritation and soft tissue impingement, making it ideal for intra-articular applications.
Moventra Medical Technology (China) Co., Ltd. stands at the forefront of this surgical manufacturing paradigm. Since our founding in 2017, we have leveraged micro-machining capabilities and Swiss-type lathe precision to design, test, and distribute class-leading compression screw systems worldwide.
| Moventra Corporate Profile & Capacity | |
|---|---|
| Established | 2017 (7 Years Export Experience) |
| Facility Area | 18,600 m² Modernized Campus |
| Annual Export | USD 23.8 Million |
| R&D Engineers | 86 Specialists |
| Quality Assurance | 48 Inspectors / 100% Pre-shipment Audit |
| Machining Capability | Swiss-Type CNC, Lathe & Milling, Wire Cutting |
| Key Markets | North America, Europe, South America, Middle East |
Acutrak and headless cannulated compression screws are critical elements in orthopedic trauma and reconstructive surgery. Here is where precision meets localized medical demand.
The scaphoid is highly susceptible to nonunion due to retrograde blood flow. The headless profile of Acutrak screws allows surgeons to insert them fully below the articular cartilage of the wrist, securing stable, compression-driven union without hindering range of motion.
Often used in radial head, distal ulna, and osteochondral fractures. The tapered thread geometry ensures that axial compressive load is distributed evenly along the screw axis, preventing stress concentration in fragile bone fragments.
Ideal for bunionectomies (lapidus arthrodesis) and triple arthrodesis. The high torsional strength of titanium alloy (Ti-6Al-4V ELI) resists micro-shearing forces in weight-bearing small bones during early recovery phases.
The global market for trauma fixation devices is shifting from traditional plate systems toward minimally invasive solutions. Headless compression screws represent a high-margin product sector driven by demographic aging, active lifestyle sports injuries, and a rising preference for outpatient surgical procedures. Medical buyers require reliable OEM/ODM partners capable of producing high-precision implants that meet rigid biomechanical benchmarks. Moventra bridges this gap by offering medical-grade raw material traceability, advanced machining, and compliance-ready manufacturing lines.
Our 18,600 m² state-of-the-art facility integrates high-precision Swiss-type CNC centers and coordinate measuring machines to meet tight dimensional tolerances (±0.005 mm).
Why international brands, hospitals, and distributors choose Moventra as their clinical orthopedic device manufacturer in China.
We work closely with ISO-certified titanium mills to source implant-grade Ti-6Al-4V ELI (Grade 23). Our structured supplier network prevents lead time volatility and minimizes material waste.
Quality control is handled by 48 QA/QC professionals. We employ dimensional verification, mechanical fatigue profiling, and laser microscopic examination to guarantee zero-defect shipments.
Supported by 86 design engineers, we offer drawing-based manufacturing, rapid functional prototyping, custom thread styling, and bespoke packaging configurations for global brands.
The evolution of trauma fixation demands smarter materials and improved bio-integration. Moventra is actively investing in research to redefine the performance boundaries of micro-fixation implants:
Our regulatory pathway aligns with demanding regional frameworks. By adhering strictly to ISO 13485 (Medical Devices Quality Management) and maintaining CE certification guidelines, we guarantee that all implants meet global biocompatibility, cleaning, and sterilization standards (including cleanroom packaging processes). This ensures a friction-free customs experience and rapid clinical adoption.
Expert engineering insights regarding Herbert and Acutrak compression screws, manufacturing specifications, and clinical applications.
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