# K110062: Mediplus-Foam AG; Mediplus-Comfortfoam AG; Mediplus-Superfoam AG

- Pathway: 510(k) (Traditional)
- Applicant: Medipurpose Pte., Ltd.
- Decided: Sep 1, 2011 after 234 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: 3 generations back to K000051 (2000). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063835: Allevyn AG Dressing, Smith & Nephew, Inc. (2007) Summary page 1.

## Most influential descendants
- K141619: Luofucon Silver Foam Dressing (2015), 0 descendants of its own

## Indications for use
The MediPlus-FoamTM AG, MediPlus-ComfortFoamTM AG, and MediPlus-SuperFoamTM AG Dressings are indicated for exudate absorption and the management of partial to full thickness wounds. Some typical wounds are: *Ulcers (venous, arterial, diabetic) *Pressure Sores *Donor Sites *Surgical Incisions *Surgical Excisions *Burns (1st and 2nd degree)

Source page: https://510kreport.com/device/K110062
Methodology: https://510kreport.com/methodology