Sinaptic Surgical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sinaptic Surgical - FDA 510(k) Cleared Devices
Recent clearances: Osteotomy Wedge System
1
Total
1
Cleared
0
Denied
Sinaptic Surgical has 1 FDA 510(k) cleared medical devices. Based in Slat Lake City, US.
Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Sinaptic Surgical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sinaptic Surgical
1 devices