Medical Device Manufacturer · FR , Montbonnot-Saint-Martin

Stryker Corporation (Tornier, S.A.S.) - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2024
2
Total
2
Cleared
0
Denied

Stryker Corporation (Tornier, S.A.S.) has 2 FDA 510(k) cleared medical devices. Based in Montbonnot-Saint-Martin, FR.

Latest FDA clearance: Apr 2026. Active since 2024. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Stryker Corporation (Tornier, S.A.S.) Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Stryker Corporation (Tornier, S.A.S.)
2 devices
1-2 of 2
Filters
All2 Orthopedic 2