Enbio Group AG - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Enbio Group AG has 3 FDA 510(k) cleared medical devices. Based in Oensingen, CH.
Latest FDA clearance: Feb 2026. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Enbio Group AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
3 devices