# K083102: Refine Lift System

- Pathway: 510(k) (Traditional)
- Applicant: Alure Medical, Inc.
- Decided: May 11, 2009 after 203 days
- Product code: FTL (Mesh, Surgical, Polymeric)
- 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: 2 generations back to K992189 (1999). 7 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K080216: Supramesh Extra, S. Jackson, Inc. (2008) Summary page 1.
- K081069: Gore Infinit Mesh, W. L. Gore & Associates, Inc. (2008) Summary page 1.
- K001122: Prolene Soft (Polypropylene), Nonabsorbabale Synthetic Surgical Mesh, ETHICON, Inc. (2000)

## Most influential descendants
- K092538: Refine Support System, Model 100.0100 (2010), 0 descendants of its own

## Indications for use
The RefineTM Support System is indicated for reinforcement of soft tissue in plastic or reconstructive procedures.

Source page: https://510kreport.com/device/K083102
Methodology: https://510kreport.com/methodology