LEM Surgical AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
LEM Surgical AG - FDA 510(k) Cleared Devices
Recent clearances: Dynamis Robotic Surgical System
2
Total
2
Cleared
0
Denied
LEM Surgical AG has 2 FDA 510(k) cleared medical devices. Based in Bern, CH.
Latest FDA clearance: Jun 2026. Active since 2025. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by LEM Surgical AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by RQM+ as regulatory consultant.
FDA 510(k) Regulatory Record - LEM Surgical AG
2 devices