FDA 510(k) Applications Submitted by Bionova Medical, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K240298 02/01/2024 Foundation Dermal Regeneration Scaffold Plus (DRS+) Duo Bionova Medical, Inc.
K231937 06/30/2023 Foundation Dermal Regeneration Scaffold (DRS) Solo Bionova Medical, Inc.
K243181 09/30/2024 Foundation Dermal Regeneration Scaffold Plus (DRS+) Solo Bionova Medical, Inc.


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