# K091863: Awbat-S Plus, Awbat-D Plus, Awbat-M Plus

- Pathway: 510(k) (Traditional)
- Applicant: Aubrey, Inc.
- Decided: Jan 21, 2010 after 212 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: 1 generation back to K082869 (2009). 1 ancestor in all.
2 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082869: Awbat-S, Awbat-D, Awbat-M, Aubrey, Inc. (2009) Summary page 3.

## Most influential descendants
- K153678: PermeaDerm B, PermeaDerm CW, and PermeaDerm Glove (2016), 1 descendant of its own
- K212579: FortiShield (Biosynthetic Wound Matrix) (2023), 0 descendants of its own

## Indications for use
AWBAT-S Plus: is intended for clean Superficial bum wounds. AWBAT-D Plus: are intended for Donor sites after hemnostasis has been established. AWBAT-M Plus: are intended to be used as a protective covering for Meshed autografts.

Source page: https://510kreport.com/device/K091863
Methodology: https://510kreport.com/methodology