Talymed
FDA 510(k) K102002 · Marine Polymer Technologies
510(k) numberK102002
Submission
- Device name
- Talymed
- Applicant
- Marine Polymer Technologies
Danvers, MA, US - Received
- July 15, 2010
- Decision date
- July 28, 2010
- 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 |
|---|---|---|
| K160695 | Talymed SuspensionFRO · Traditional | 12/06/2016SE |
| K132293 | Syvek Radial BandDXC · Traditional | 07/31/2014SE |
| K111524 | MP 719MTJ · Traditional | 07/22/2011SE |
| K082703 | MRDH BandageKMF · Traditional | 10/14/2008SE |
| K070557 | MP 719FRO · Traditional | 05/23/2007SE |
| K053300 | SyvekexcelDXC · Traditional | 03/28/2006SE |
| K002550 | RDH BandageKMF · Traditional | 12/20/2000SE |
| K984177 | Modification to SkvekpatchKMF · Traditional | 12/18/1998SN |
| K972914 | Syvek PatchKGX · Traditional | 12/22/1997SE |
Questions and answers
When was Talymed cleared by the FDA?
Talymed (K102002) received a 510(k) decision of Substantially Equivalent on July 28, 2010, 13 days after the submission was received.
What is the product code of K102002?
The FDA product code is FRO – Dressing, Wound, Drug, a Unclassified device.