Wright Medical Technology, Inc. (Stryker) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Wright Medical Technology, Inc. (Stryker) - FDA 510(k) Cleared Devices
Recent clearances: Incompass Total Ankle System, Prophecy Surgical Planning System
2
Total
2
Cleared
0
Denied
Wright Medical Technology, Inc. (Stryker) has 2 FDA 510(k) cleared medical devices. Based in Memphis, US.
Latest FDA clearance: Jun 2025. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Wright Medical Technology, Inc. (Stryker) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Wright Medical Technology, Inc. (Stryker)
2 devices