# K223482: reVive Light Therapy® Wrinkle and Acne LED Device

- Pathway: 510(k) (Special)
- Applicant: Led Technologies, Inc.
- Decided: Dec 21, 2022 after 33 days
- Product code: OHS (Light Based Over The Counter Wrinkle Reduction)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 16 generations back to K943450 (1995). 125 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 128 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K210965: reVive Light Therapy Essentials, Led Technologies, Inc. (2021) Summary page 5.
- K210968: reVive Light Therapy Essentials, Led Technologies, Inc. (2021) Summary page 5.

## Most influential descendants
- K243587: PureLift GLOW (2025), 1 descendant of its own
- K261370: LED Light Therapy Masks (LED Face Mask Pulse (FAC06NA)) (2026), 0 descendants of its own

## Indications for use
The reVive Light Therapy® Wrinkle and Acne LED Device is intended for treatment of wrinkles and mild to moderate inflammatory acne.

Source page: https://510kreport.com/device/K223482
Methodology: https://510kreport.com/methodology