# K070557: MP 719

- Pathway: 510(k) (Traditional)
- Applicant: Marine Polymer Technologies, Inc.
- Decided: May 23, 2007 after 85 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: 4 generations back to K881854 (1988). 13 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K984177: Modification to Skvekpatch, Marine Polymer Technologies, Inc. (1998) Summary page 1.
- K002550: RDH Bandage, Marine Polymer Technologies, Inc. (2000) Summary page 1.
- K061060: TT101, Models TT 101-1,-2,-3,-4,-5,-6,-7,-8, Tissue Technologies Holdings, LLC (2006)
- K023778: Dressskin, Tei Biosciences, Inc. (2003)
- K014129: Promogran Matrix Wound Dressing, Johnson & Johnson Medical, Ltd. (2002)

## Cited in the summary but kept off the family tree
- K022673: Sy-vekNT. Not in FDA’s 510(k), De Novo or PMA lists as we hold them (a misreading, a typo, or a number FDA does not list), so it is kept off the family tree Summary page 1.

## Most influential descendants
- K111524: MP 719 (2011), 0 descendants of its own
- K102002: Talymed (2010), 0 descendants of its own

## Indications for use
TALIDERM Tm 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, and other bleeding surface wounds Abrasions Traumatic wounds healing by secondary intention Dehisced surgical wounds. TALIDERM Tm is intended for use under the direction of a healthcare professional,

Source page: https://510kreport.com/device/K070557
Methodology: https://510kreport.com/methodology