Bionova Medical, Inc.
Bionova Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2012, most recent 2024.
Top product codes for Bionova Medical, Inc.
Recent clearances by Bionova Medical, Inc.
- K243181 — Foundation Dermal Regeneration Scaffold Plus (DRS+) Solo
- K240298 — Foundation Dermal Regeneration Scaffold Plus (DRS+) Duo
- K231937 — Foundation Dermal Regeneration Scaffold (DRS) Solo
- K210949 — Foundation Dermal Regeneration Scaffold (DRS) Solo
- K123961 — SENTREX BIOSPONGE MPD
- K112191 — HEALEX BIOSPONGE WOUND DRESSING
Data sourced from openFDA. This site is unofficial and independent of the FDA.