# K250227: JOVS Electric Stimulation Beauty Device (JE2)

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Qianyu Technology Co., Ltd.
- Decided: Oct 17, 2025 after 263 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: 6 generations back to K011935 (2001). 9 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K233010: Beagank 4T Plus, Belega, Inc. (2023) Summary page 5.
- K103031: BMR Face, Bio-Medical Research, Ltd. (2011) Summary page 5.
- K011935: Rejuvenique Model #RJV10, Salton, Inc. (2001) Summary page 5.

## Most influential descendants
- K253932: FACEGYM Pro Device (HD-109) (2026), 0 descendants of its own

## Indications for use
JOVS Electric Stimulation Beauty Device is indicated for over-the-counter aesthetic use including facial and neck stimulation.

Source page: https://510kreport.com/device/K250227
Methodology: https://510kreport.com/methodology