Stryker Trauma AG
Also registered as Stryker Trauma GmbH
Country not established FDA
- Devices
- 357
- Registrations
- FDA
- FDA recalls
- 0
What Stryker Trauma AG makes
Stryker Trauma AG manufactures orthopedic fixation devices, including pelvic implants, locking plate systems for limb reconstruction, wrist and clavicle fusion plates, and intramedullary nailing systems for tibial fractures. Their portfolio also covers reversible fracture systems, shoulder arthroplasty components, and modular limb reconstruction frames designed for complex bone repairs.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company’s products are listed in the FDA’s 510(k) clearance registry, reflecting compliance with US medical device regulations. The manufacturer is based in the United States.
Catalogue
Search and filter all 357 devicesShowing 101-150 of 357
FDA establishments
- Stryker Trauma GmbH SCHOENKIRCHEN Schleswig-Holstein · DE FEI 3002807231