Feops NV - FDA 510(k) Cleared Devices

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.

510(k) submissions have been managed by Orthogrow NV as regulatory consultant.