Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Silhouette Lift, Inc. · Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
66 daysmedian FDA review time
268 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K200140 | Silhouette Instalift | Silhouette Lift, Inc. | 2020-03-27 | 66 | 0 |
| K191299 | Silhouette Featherlift / Silhouette Lift | Silhouette Lift, Inc. | 2019-06-14 | 31 | 0 |
| K163676 | Silhouette InstaLift | Silhouette Lift, Inc. | 2017-06-16 | 171 | 0 |
| K171005 | Silhouette Featherlift | Silhouette Lift, Inc. | 2017-05-03 | 29 | 0 |
| K142061 | SILHOUETTE INSTALIFT | Silhouette Lift, Inc. | 2015-04-24 | 268 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda