# K133896: Rejuvalite MD

- Pathway: 510(k) (Traditional)
- Applicant: Trophy Skin, Inc.
- Decided: Nov 13, 2014 after 328 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: 2 generations back to K101190 (2010). 2 ancestors in all.
105 later devices descend from it; 6 cite it directly.
0 of 108 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K120775: Light for Wrinkles, Led Intellectual Properties, LLC (2012) Summary page 5.

## Most influential descendants
- K170984: LG Beauty Led Mask (2017), 93 descendants of its own
- K191629: faceLITE (2019), 71 descendants of its own
- K183671: LG Pra.L Derma Led Mask (2019), 48 descendants of its own
- K180856: Neutrogena Light Therapy Aging Mask+ (2018), 45 descendants of its own
- K190443: MMSphere (2019), 42 descendants of its own

## Indications for use
The Rejuvalite MD is an Over the Counter device that is intended for the use in the treatment of full face wrinkles.

Source page: https://510kreport.com/device/K133896
Methodology: https://510kreport.com/methodology