K260511
- 510(k) number
- K260511
- Device name
- Ulike Reglow Light Therapy Device (UM10)
- Applicant
- Shenzhen Ulike Smart Electronics Co., Ltd. CN
- Product code
- OHS — Light Based Over The Counter Wrinkle Reduction
- Decision date
- 2026-03-16
- Date received
- 2026-02-17
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K260511.pdf
Official FDA record: K260511
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.