Stryker Trauma AG
Country not established FDA
- Devices
- 357
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
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 1-50 of 357
FDA establishments
- Stryker Trauma GmbH SCHOENKIRCHEN Schleswig-Holstein · DE FEI 3002807231
Frequently asked questions
How many devices does Stryker Trauma AG have in the registry?
The registry currently lists 357 devices for Stryker Trauma AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stryker Trauma AG's devices?
Among its 50 most recently registered devices, Stryker Trauma AG has devices listed in FDA GUDID (50 devices).
What risk classes do Stryker Trauma AG's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Stryker Trauma AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stryker Trauma AG in the registry?
The most recently registered devices listed for Stryker Trauma AG include NA 1796-4050S, S2 1735-1340S, S2 1795-5075S and S2 1722-1130S.
Which FDA establishments are linked to Stryker Trauma AG?
1 FDA establishment is linked to Stryker Trauma AG in the registry; they are listed on the company page.