Relu BV is one of 33 FDA 510(k) medical device manufacturers from Belgium in the dataset, ranked by real submission volume.
Relu BV - FDA 510(k) Cleared Devices
Recent clearances: Relu Cloud, Relu Creator
2
Total
2
Cleared
0
Denied
Relu BV has 2 FDA 510(k) cleared medical devices. Based in Leuven, BE.
Latest FDA clearance: Apr 2026. Active since 2024. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Relu BV Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Prime Path Medtech as regulatory consultant.
FDA 510(k) Regulatory Record - Relu BV
2 devices