K251825
- 510(k) number
- K251825
- Device name
- Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG)
- Applicant
- Shenzhen Ulike Smart Electronics Co., Ltd. CN
- Product code
- OHS — Light Based Over The Counter Wrinkle Reduction
- Decision date
- 2025-10-01
- Date received
- 2025-06-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 3.1 MB · U.S. public domain
Also available from FDA: K251825.pdf
Official FDA record: K251825
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.