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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.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue357

Newest first, rows 351-357 of 357

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  • AxSOS 3 Ti Locking Plate System Ref K143138

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Asnis JFX System Ref K153154

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Fixos Screw System Ref K133451

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Hoffmann Lrf (Limb Reconstruction Frame) System Ref K130907

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Axsos 3 Ti Locking Plate System Ref K123964

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Gamma3 System Ref K200869

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Variax Elbow Plating System Ref K141677

    Active Regimes: 510(k) Registry: 510(k) Class:II

Showing 351-357 of 357

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Stryker Trauma GmbH SCHOENKIRCHEN Schleswig-Holstein · DE FEI 3002807231