# K240360: Wrinkle Treatment Device (JM2)

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Qianyu Technology Co., Ltd.
- Decided: Apr 5, 2024 after 59 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: 17 generations back to K943450 (1995). 176 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 179 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K230293: TheraFace Mask, Therabody, Inc. (2023) Summary page 5.
- K210954: Synergy, Yrs Group, Inc. (2021) Summary page 5.
- K162489: RED Light Device, Zhongshan Bisen Plastic Electronic Products Co., Ltd. (2017) Summary page 5.

## Most influential descendants
- K261370: LED Light Therapy Masks (LED Face Mask Pulse (FAC06NA)) (2026), 0 descendants of its own
- K244020: Wrinkle Treatment Device (JM1, JM2B) (2025), 0 descendants of its own

## Indications for use
The wrinkle treatment device (model: JM2) is an Over-the-Counter (OTC) light based device intended for the use in treating full-face wrinkles.

Source page: https://510kreport.com/device/K240360
Methodology: https://510kreport.com/methodology