# K200140: Silhouette Instalift

- Pathway: 510(k) (Traditional)
- Applicant: Silhouette Lift, Inc.
- Decided: Mar 27, 2020 after 66 days
- Product code: GAM (Suture, Absorbable, Synthetic, Polyglycolic Acid)
- Device class: 2
- Regulation: 21 CFR 878.4493
- 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 K142061 (2015). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K142061: Silhouette Instalift, Silhouette Lift, Inc. (2015) Summary page 5.
- K163676: Silhouette InstaLift, Silhouette Lift, Inc. (2017) Summary page 4.

## Indications for use
The Silhouette Instalift device is indicated for use in mid-face suspension surgery to temporarily fixate the cheek sub dermis in an elevated position.

Source page: https://510kreport.com/device/K200140
Methodology: https://510kreport.com/methodology