# K210968: reVive Light Therapy Essentials

- Pathway: 510(k) (Traditional)
- Applicant: Led Technologies, Inc.
- Decided: Dec 21, 2021 after 265 days
- Product code: OLP (Over-The-Counter Powered Light Based Laser For Acne)
- 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: 15 generations back to K943450 (1995). 111 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 115 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K180447: reVive Light Therapy LED Cleansing System, Led Technologies, Inc. (2018) Summary page 5.
- K180320: dpl IIa Panel, Led Technologies, Inc. (2018) Summary page 5.

## Most influential descendants
- K223482: reVive Light Therapy® Wrinkle and Acne LED Device (2022), 2 descendants of its own
- 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® Essentials is an Over the Counter (OTC) device intended for treatment of mild to moderate inflammatory acne.

Source page: https://510kreport.com/device/K210968
Methodology: https://510kreport.com/methodology