Comerge AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Comerge AG - FDA 510(k) Cleared Devices
Recent clearances: T1D1, Neo ADVISE software
2
Total
2
Cleared
0
Denied
Comerge AG has 2 FDA 510(k) cleared medical devices. Based in Zurich, CH.
Latest FDA clearance: Aug 2025. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Comerge AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Confinis AG as regulatory consultant.
FDA 510(k) Regulatory Record - Comerge AG
2 devices