Bionova Medical, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Bionova Medical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Alexandria, US.
Latest FDA clearance: Oct 2024. Active since 2012. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Bionova Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Bionova Medical, Inc.
6 devices
Cleared
Oct 31, 2024
Foundation Dermal Regeneration Scaffold Plus (DRS+) Solo
General & Plastic Surgery
31d
Cleared
Aug 21, 2024
Foundation Dermal Regeneration Scaffold Plus (DRS+) Duo
General & Plastic Surgery
202d
Cleared
Nov 13, 2023
Foundation Dermal Regeneration Scaffold (DRS) Solo
General & Plastic Surgery
136d
Cleared
Aug 11, 2022
Foundation Dermal Regeneration Scaffold (DRS) Solo
General & Plastic Surgery
499d
Cleared
Apr 05, 2013
SENTREX BIOSPONGE MPD
General & Plastic Surgery
100d
Cleared
Jun 05, 2012
HEALEX BIOSPONGE WOUND DRESSING
General & Plastic Surgery
312d