# K130852: Avance® Foam Abdominal Dressing Kit

- Pathway: 510(k) (Traditional)
- Applicant: Molnlycke Health Care
- Decided: Apr 14, 2014 after 382 days
- Product code: OXJ (Mesh, Surgical, Non-Absorbable, Large Abdominal Wall Defects)
- Device class: 2
- Regulation: 21 CFR 878.3300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K945062 (1995). 16 ancestors in all.
3 later devices descend from it; 2 cite it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K122132: Avance Foam Dressing Kit Incl. Transparent Film, Transfer Pad (Small, Medium, Large) Avance Transparent Film Avance Foam, Molnlycke Health Care (2013) Summary page 1.
- K112784: Renasys AB Abominal Dressing Kit, Smith & Nephew, Inc. (2011) Summary page 1.

## Most influential descendants
- K161939: Avance Abdominal Dressing Kit (2016), 1 descendant of its own
- K182722: XLR8 Abdominal Wound Dressing Kit (2019), 0 descendants of its own
- K182191: Invia Abdominal Dressing Kit (2019), 0 descendants of its own

## Indications for use
The Avance® Foam Abdominal Dressing Kit is indicated for temporary bridging of abdominal wall openings where primary closure is not possible and/or repeat abdominal entries may be required. Its intended use is with patients who have open abdominal wounds with exposed viscera and organs, and including but not limited to patients with abdominal compartment syndrome. It is intended for use in acute hospital settings (trauma, general and plastic surgery wards) and should ideally be applied in the operating theatre. The dressing kit is intended for use together with the Avance NPWT pump and its accessories.

Source page: https://510kreport.com/device/K130852
Methodology: https://510kreport.com/methodology