Feops NV is one of 33 FDA 510(k) medical device manufacturers from Belgium in the dataset, ranked by real submission volume.
Feops NV - FDA 510(k) Cleared Devices
Recent clearances: FEops HEARTguide Simulation Application, FEops HEARTguideTM, FEops HEARTguideTM ALPACA, FEops HEARTguide
4
Total
3
Cleared
1
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.
510(k) submissions have been managed by Orthogrow NV as regulatory consultant.
FDA 510(k) Regulatory Record - Feops NV
4 devices