Silhouette Lift, Inc.

FDA Regulatory Profile

Silhouette Lift, Inc. appears in FDA public data with 1 recall, 5 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2208-2015, Class II) was initiated on July 2, 2015. Its most recent 510(k) clearance was granted on March 27, 2020.

Summary

Total Recalls
1
510(k) Clearances
5
Inspections
3
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-2208-2015Class IISilhouette Lift brochure Silhouette Sutures are for use in midface suspension surgery to fixate tJuly 2, 2015

Recent 510(k) Clearances

K-NumberDeviceDate
K200140Silhouette InstaliftMarch 27, 2020
K191299Silhouette Featherlift / Silhouette LiftJune 14, 2019
K163676Silhouette InstaLiftJune 16, 2017
K171005Silhouette FeatherliftMay 3, 2017
K142061SILHOUETTE INSTALIFTApril 24, 2015