Replasia BV is one of 46 FDA 510(k) medical device manufacturers from Belgium in the dataset, ranked by real submission volume.
Replasia BV - FDA 510(k) Cleared Devices
Recent clearances: HipStudio Analysis
1
Total
1
Cleared
0
Denied
Replasia BV has 1 FDA 510(k) cleared medical devices. Based in Leuven, BE.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Replasia BV Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Aucto BV as regulatory consultant.
FDA 510(k) Regulatory Record - Replasia BV
1 devices