Medical Device Manufacturer · US , Irvine , CA

Silhouette Lift, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2015

Total

Cleared

Denied

Silhouette Lift, Inc. has 5 FDA 510(k) cleared medical devices. Based in Irvine, US.

Historical record: 5 cleared submissions from 2015 to 2020. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Silhouette Lift, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Health Policy Associates, Inc. as regulatory consultant.

Silhouette Lift, Inc. is one of 13157 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Silhouette Lift, Inc.

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: May 28, 2026