Revisios BV is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Revisios BV - FDA 510(k) Cleared Devices
Recent clearances: OsOpia Synthetic Bone Void Filler
1
Total
1
Cleared
0
Denied
Revisios BV has 1 FDA 510(k) cleared medical devices. Based in 3723 Mb Bilthoven, NL.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Revisios BV Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MRC Global as regulatory consultant.
FDA 510(k) Regulatory Record - Revisios BV
1 devices