Medical Device Manufacturer · BE , Gent-Zwijnaarde

Feops NV - FDA 510(k) Cleared Devices

4 submissions · 3 cleared · Since 2021

Total

Cleared

Denied

Feops NV has 3 FDA 510(k) cleared medical devices. Based in Gent-Zwijnaarde, BE.

Latest FDA clearance: Nov 2025. Active since 2021. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Feops NV Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Feops NV

4 devices

1-4 of 4