Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list LED Technologies with 15 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Dec 21, 2022: reVive Light Therapy® Wrinkle and Acne LED Device.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Dec 21, 2022 | reVive Light Therapy® Wrinkle and Acne LED DeviceK223482 · OHS | 510(k) clearances |
| Jul 27, 2022 | reVive Light Therapy LED Cleansing SystemK221430 · OHS | 510(k) clearances |
| Dec 21, 2021 | reVive Light Therapy EssentialsK210968 · OLP | 510(k) clearances |
| Dec 15, 2021 | reVive Light Therapy EssentialsK210965 · OHS | 510(k) clearances |
| Mar 14, 2019 | dpl FacewareK183247 · OHS | 510(k) clearances |
| Feb 7, 2019 | dpl SpotLiteK183118 · OLP | 510(k) clearances |
| Jun 4, 2018 | reVive Light Therapy LED Cleansing SystemK180447 · OLP | 510(k) clearances |
| May 15, 2018 | reVive Light Therapy LED Ultrasonic Wrinkle SystemK180445 · OHS | 510(k) clearances |
| Mar 30, 2016 | reVive Light Therapy Pain Relief Device (Model Number: RVPNSYS) Product Usage: The reVive Light Therapy Pain Relief Device is a deviceClass II · Incorrect Power Supply in the package, rendering the device inoperable. | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
