# K260020: Redermo Wound Matrix

- Pathway: 510(k) (Traditional)
- Applicant: Beijing Kreate Medical Co., Ltd.
- Decided: Apr 16, 2026 after 101 days
- Product code: QSZ (Absorbable Synthetic Wound Dressing)
- 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: 10 generations back to K842066 (1985). 82 ancestors in all.
No later device cites it as a predicate yet.
0 of 83 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K170300: Restrata Wound Matrix, Acera Surgical, Inc. (2017) Summary page 5.

## Indications for use
The product is intended for use in the management of wounds, including: Partial and full thickness wounds, pressure sores/ulcers, venous ulcers, diabetic ulcers, chronic vascular ulcers, tunneled/undermined wounds, surgical wound (e.g., donor site/grafts, post-laser surgery, post Mohs surgery, podiatric wounds, dehisced wounds), trauma wounds (e.g., abrasions, lacerations, partial thickness burns, skin tears), and draining wounds.

Source page: https://510kreport.com/device/K260020
Methodology: https://510kreport.com/methodology