K261407
- 510(k) number
- K261407
- Device name
- XPREEN LED Light Therapy Masks (XPRE322, XPRE326, XPRE327, XPRE342, XPRE368, XPRE422, XPRE434, XPRE451, XPRE455, XPRE457, XPRE448, XPRE335, XPRE350, XPRE420, XPRE436, XPRE339, XPRE445)
- Applicant
- Dongguan Miqiang Technology Co., Ltd. CN
- Product code
- OHS — Light Based Over The Counter Wrinkle Reduction
- Decision date
- 2026-07-15
- Date received
- 2026-04-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 3.0 MB · U.S. public domain
Also available from FDA: K261407.pdf
Official FDA record: K261407
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.