Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Led Technologies, Inc. — Predicate Candidate Screening
12 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
90 daysmedian FDA review time
259 days90th percentile
12clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K223482 | reVive Light Therapy® Wrinkle and Acne LED Device | Led Technologies, Inc. | 2022-12-21 | 33 | 0 |
| K221430 | reVive Light Therapy LED Cleansing System | Led Technologies, Inc. | 2022-07-27 | 71 | 0 |
| K210968 | reVive Light Therapy Essentials | Led Technologies, Inc. | 2021-12-21 | 265 | 0 |
| K210965 | reVive Light Therapy Essentials | Led Technologies, Inc. | 2021-12-15 | 259 | 0 |
| K183247 | dpl Faceware | Led Technologies, Inc. | 2019-03-14 | 113 | 0 |
| K183118 | dpl SpotLite | Led Technologies, Inc. | 2019-02-07 | 90 | 0 |
| K180447 | reVive Light Therapy LED Cleansing System | Led Technologies, Inc. | 2018-06-04 | 104 | 0 |
| K180445 | reVive Light Therapy LED Ultrasonic Wrinkle System | Led Technologies, Inc. | 2018-05-15 | 84 | 0 |
| K180320 | dpl IIa Panel | Led Technologies, Inc. | 2018-04-03 | 57 | 0 |
| K172662 | reVive Perioral | Led Technologies, Inc. | 2018-01-09 | 126 | 0 |
| K171386 | dpl SpectraLite | Led Technologies, Inc. | 2017-08-07 | 88 | 0 |
| K171390 | dpl II Panel | Led Technologies, Inc. | 2017-08-03 | 84 | 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