Foundation Dermal Regeneration Scaffold Plus (DRS+) Duo
FDA 510(k) K240298 · Bionova Medical, Inc.
510(k) numberK240298
Submission
- Device name
- Foundation Dermal Regeneration Scaffold Plus (DRS+) Duo
- Applicant
- Bionova Medical, Inc.
Germantown, TN, US - Received
- February 1, 2024
- Decision date
- August 21, 2024
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- FRO – Dressing, Wound, Drug
- Device class
- Unclassified
Other 510(k)s with product code FRO
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K254041 | SkinSmart Antimicrobial HydroGelFRO · Traditional | Magic Science Supply, LLC | 09/11/2026SE |
| K261646 | Redermax® Antibacterial Wound MatrixFRO · Traditional | Beijing Kreate Medical Co., Ltd. | 08/14/2026SE |
| K253665 | Vashe Plus Antimicrobial SolutionFRO · Traditional | Urgo Medical North America, LLC | 08/11/2026SE |
| K261023 | Microdacyn Wound Irrigation SolutionFRO · Traditional | Sonoma Pharmaceuticals, Inc. | 06/24/2026SE |
| K251929 | SilverCeuticals® Antimicrobial Wound GelFRO · Traditional | Silverceuticals, Inc. | 06/24/2026SE |
| K261638 | Bonvadis®FRO · Special | Oneness Biotech Co., Ltd. | 06/17/2026SE |
| K254073 | StatSeal DiscFRO · Traditional | Merit Medical Systems, Inc. | 05/13/2026SE |
| K254191 | IWD-GelFRO · Traditional | InnovaCorium, Inc. | 04/07/2026SE |
| K252023 | MiraChlor Antimicrobial Wound SolutionFRO · Traditional | Letus Corporation | 03/25/2026SE |
| K251999 | Promogran Prisma Collagen Matrix with ORC and SilverFRO · Traditional | Solventum Germany GmbH | 03/13/2026SE |
More from Solventum Germany GmbH
| 510(k) | Device | Decision |
|---|---|---|
| K243181 | Foundation Dermal Regeneration Scaffold Plus (DRS+) SoloFRO · Special | 10/31/2024SE |
| K231937 | Foundation Dermal Regeneration Scaffold (DRS) SoloKGN · Traditional | 11/13/2023SE |
| K210949 | Foundation Dermal Regeneration Scaffold (DRS) SoloKGN · Traditional | 08/11/2022SE |
| K123961 | Sentrex Biosponge MPDKGN · Traditional | 04/05/2013SE |
| K112191 | Healex Biosponge Wound DressingKGN · Traditional | 06/05/2012SE |
Questions and answers
When was Foundation Dermal Regeneration Scaffold Plus (DRS+) Duo cleared by the FDA?
Foundation Dermal Regeneration Scaffold Plus (DRS+) Duo (K240298) received a 510(k) decision of Substantially Equivalent on August 21, 2024, 202 days after the submission was received.
What is the product code of K240298?
The FDA product code is FRO – Dressing, Wound, Drug, a Unclassified device.