BIONOVA MEDICAL, INC.

FDA Device Registration & Listing · Germantown, TN, US · Registration 3009973323

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3009973323
FEI Number
3009973323
Entity Name
BIONOVA MEDICAL, INC.
City/State/Country
Germantown, TN, US
Establishment Address
3012 CENTRE OAK WAY STE 102, Germantown, TN 38138, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Bionova Medical, Inc. (Owner Number: 10042462)
Owner / Operator Contact Address
3012 Centre Oak Way, Suite 102, Germantown, TN 38138, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Foundation Dermal Regeneration Scaffold Plus (DRS+) Solo Foundation DRS Solo Sentrex BioSponge MPD

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FRO Dressing, Wound, Drug Unknown Class U N/A 2025-06-30
KGN Wound Dressing With Animal-Derived Material(S) Unknown Class U N/A 2025-06-30
KGN Wound Dressing With Animal-Derived Material(S) Unknown Class U N/A 2023-11-29
KGN Wound Dressing With Animal-Derived Material(S) Unknown Class U N/A 2014-01-02

Official Correspondent

Alex Greene

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Bionova Medical, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K150256 Argentum Medical SILVERLON BURN CONTACT DRESSINGS 2015-04-30
K112888 Kensey Nash Corporation MESO WOUND MATRIX 2012-02-10
K040211 Collagen Matrix, Inc. MODIFICATION TO: COLLAGEN TOPICAL WOUND DRESSING 2004-02-27

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0003-06 B. Braun Medical, Inc. U
D-Stat Dry Hemostatic Bandage. The product is an adhesive bandage.
Z-0038-2025 3M Company Health Care Business 3m Center U
3M Tegaderm CHG, Chlorhexidine Gluconate I.V. Securement Dressing, REF 1658R

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009973323. Last updated year: 2026. Please use registration number 3009973323 when referencing this establishment in official correspondence.
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