Bioncise NV is one of 33 FDA 510(k) medical device manufacturers from Belgium in the dataset, ranked by real submission volume.
Bioncise NV - FDA 510(k) Cleared Devices
Recent clearances: Spirotome Endo 08 Gauge, Spirotome Endo 10 Gauge, Spirotome Endo 14 Gauge, Spirotome Endo 14 Gauge with 10 mm Helix
1
Total
1
Cleared
0
Denied
Bioncise NV has 1 FDA 510(k) cleared medical devices. Based in Wellen, BE.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Bioncise NV Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bioncise NV
1 devices