# Alure Medical, Inc.

- Location (FDA's records): Carlsbad, CA
- FDA decisions: 2 (2009–2010): 2 510(k) clearances
- Product codes: FTL (2)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- S. Jackson, Inc.: 1 (https://510kreport.com/company/s-jackson)
- W. L. Gore & Associates, Inc.: 1 (https://510kreport.com/company/w-l-gore-associates)
- ETHICON, Inc.: 1 (https://510kreport.com/company/ethicon)

## Its most-cited devices
- K083102: Refine Lift System (2009), cited by 1

## Recent decisions
- K092538: Refine Support System, Model 100.0100 (Mar 5, 2010)
- K083102: Refine Lift System (May 11, 2009)

Source page: https://510kreport.com/company/alure-medical