# K251825: Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG)

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Ulike Smart Electronics Co., Ltd.
- Decided: Oct 1, 2025 after 110 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). 286 ancestors in all.
No later device cites it as a predicate yet.
0 of 287 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K223919: B.Light Clear Evo and B.Light Restore Evo, Bemer Int AG (2023) Summary page 5.
- K210948: Omnilux CLEAR, Globalmed Technologies (2021) Summary page 5.
- K240089: Face Patches (MT-12MA, MT-12MC), Shenzhen Kaiyan Medical Equipment Co., Ltd. (2024) Summary page 5.

## Indications for use
Jmoon FlexGlow Light Therapy Device is an over the counter device that is intended: - the Red light and Infrared light is indicated for use in the treatment of full face wrinkles, - the Blue light and Red light indicated for the treatment of mild to moderate inflammatory acne.

Source page: https://510kreport.com/device/K251825
Methodology: https://510kreport.com/methodology