# Silhouette Lift, Inc.

- Location (FDA's records): Irvine, CA
- FDA decisions: 5 (2015–2020): 5 510(k) clearances
- Product codes: GAM (3), GAW (2)
- 510(k) review time since 2016: median 66 days, against 140 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 6 (4 its own); citations of its devices by later devices: 5 (4 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
- Kmi Kolster Methods, Inc.: 2 (https://510kreport.com/company/kmi-kolster-methods)

## Firms that cite its devices most
- Hans Biomed Corporation: 1 (https://510kreport.com/company/hans-biomed)

## Its most-cited devices
- K142061: Silhouette Instalift (2015), cited by 2
- K163676: Silhouette InstaLift (2017), cited by 2
- K171005: Silhouette Featherlift (2017), cited by 1

## Recent decisions
- K200140: Silhouette Instalift (Mar 27, 2020)
- K191299: Silhouette Featherlift / Silhouette Lift (Jun 14, 2019)
- K163676: Silhouette InstaLift (Jun 16, 2017)
- K171005: Silhouette Featherlift (May 3, 2017)
- K142061: Silhouette Instalift (Apr 24, 2015)

Source page: https://510kreport.com/company/silhouette-lift