# K102002: Talymed

- Pathway: 510(k) (Traditional)
- Applicant: Marine Polymer Technologies
- Decided: Jul 28, 2010 after 13 days
- Product code: FRO (Dressing, Wound, Drug)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K881854 (1988). 15 ancestors in all.
No later device cites it as a predicate yet.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070557: MP 719, Marine Polymer Technologies, Inc. (2007) Summary page 1.
- K061711: Oasis Wound Matrix, Cook Biotech, Inc. (2006) Summary page 1.

## Indications for use
TalymedTM is indicated for the management of wounds including: Diabetic ulcers Venous ulcers Pressure wounds Ulcers caused by mixed vascular etiologies Full thickness and partial thickness wounds Second degree burns Surgical wounds-donor sites/grafts, post-mohr's surgery, post-laser surgery, and other bleeding surface wounds, Abrasions, lacerations Traumatic wounds healing by secondary intention Chronic vascular ulcers Dehisced surgical wounds.

Source page: https://510kreport.com/device/K102002
Methodology: https://510kreport.com/methodology