Stryker Corporation (Tornier, Inc.) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stryker Corporation (Tornier, Inc.) - FDA 510(k) Cleared Devices
Recent clearances: Tornier Humeral Reconstruction System (Tornier HRS), Tornier Humeral Reconstruction System (Tornier HRS)
3
Total
3
Cleared
0
Denied
Stryker Corporation (Tornier, Inc.) has 3 FDA 510(k) cleared medical devices. Based in Bloomington, US.
Latest FDA clearance: Jun 2026. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Stryker Corporation (Tornier, Inc.) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stryker Corporation (Tornier, Inc.)
3 devices