# K140510: Miromatrix Wound Matrix

- Pathway: 510(k) (Traditional)
- Applicant: Miromatrix Medical, Inc.
- Decided: Jun 19, 2014 after 111 days
- Product code: KGN (Wound Dressing With Animal-Derived Material(S))
- 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: 1 generation back to K061711 (2006). 1 ancestor in all.
9 later devices descend from it; 3 cite it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061711: Oasis Wound Matrix, Cook Biotech, Inc. (2006) Summary page 1.

## Most influential descendants
- K221520: Miro3D Wound Matrix (2022), 4 descendants of its own
- K223257: Miro3D Wound Matrix (2022), 3 descendants of its own
- K171842: Geistlich Wound Matrix (2017), 2 descendants of its own
- K182838: Geistlich Derma-Gide (2018), 1 descendant of its own
- K260532: Derma-Gide (2026), 0 descendants of its own

## Indications for use
The Miromatrix Wound Matrix is intended for the management of wounds including: * Partial and full thickness wounds; * Pressure ulcers; * Venous ulcers; * Diabetic ulcers; * Chronic vascular ulcers; * Tunneled, undermined wounds; * Surgical wounds (donor sites/grafts, post-Mohs' surgery, post-laser surgery, podiatric, wound dehiscence); * Trauma wounds (abrasions, lacerations, second-degree bums, and skin tears); * Draining wounds.

Source page: https://510kreport.com/device/K140510
Methodology: https://510kreport.com/methodology