# K244020: Wrinkle Treatment Device (JM1, JM2B)

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Qianyu Technology Co., Ltd.
- Decided: May 1, 2025 after 125 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: 18 generations back to K943450 (1995). 177 ancestors in all.
No later device cites it as a predicate yet.
0 of 178 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K240360: Wrinkle Treatment Device (JM2), Shenzhen Qianyu Technology Co., Ltd. (2024) Summary page 5.

## Indications for use
The Wrinkle Treatment Device is an Over-the-Counter (OTC) light based device intended for the use in treating full-face wrinkles.

Source page: https://510kreport.com/device/K244020
Methodology: https://510kreport.com/methodology