# K152199: RejuvatoneMD

- Pathway: 510(k) (Traditional)
- Applicant: Trophy Skin, Inc.
- Decided: Mar 23, 2016 after 230 days
- Product code: NFO (Stimulator, Transcutaneous Electrical, Aesthetic Purposes)
- Device class: 2
- Regulation: 21 CFR 882.5890
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K011935 (2001). 5 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K133823: Nuface Mini Device, Carol Cole Company (2014) Summary page 5.

## Most influential descendants
- K182025: ClearUP Sinus Pain Relief (2019), 0 descendants of its own

## Indications for use
The RejuvatoneMD is intended for facial stimulation and is indicated for over-the-counter cosmetic use.

Source page: https://510kreport.com/device/K152199
Methodology: https://510kreport.com/methodology