# K241080: Kerecis Parvus (50207)

- Pathway: 510(k) (Traditional)
- Applicant: Kerecis Limited
- Decided: Aug 21, 2024 after 124 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: 9 generations back to K921895 (1992). 65 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 67 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K190528: MariGen Wound Extra, Kerecis Limited (2019) Summary page 5.

## Most influential descendants
- K251845: Marigen Wound Extra; Kerecis Silicone; Kerecis Parvus (2025), 0 descendants of its own

## Indications for use
Management of wounds including: • Partial and full-thickness wounds • Pressure ulcers • Venous ulcers • Chronic vascular ulcers • Diabetic ulcers • Trauma wounds (abrasions, lacerations, partial thickness burns, skin tears) • Surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) • Draining wounds

Source page: https://510kreport.com/device/K241080
Methodology: https://510kreport.com/methodology