Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG)— 510(k) K251825

Substantially Equivalent

Shenzhen Ulike Smart Electronics Co., Ltd.

FDA 510(k) clearance K251825 for Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG), Substantially Equivalent on 2025-10-01. Applicant: Shenzhen Ulike Smart Electronics Co., Ltd..

Clearance details

Applicant: Shenzhen Ulike Smart Electronics Co., Ltd.
Product code: Code OHS
Advisory panel: General, Plastic Surgery
Date received: 2025-06-13
Decision date: 2025-10-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

Adverse events under product code OHS

product code OHS

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.