K252142
- 510(k) number
- K252142
- Device name
- Multi-functional Facial Beauty Device (SKB-1703,SKB-1803,SKB-1809, SKB-1909, SKB-2109,SKB-2129,SKB-2208PRO, SKB-2209)
- Applicant
- Shenzhen Siken 3D Technology Development Co., Ltd. CN
- Product code
- OHS — Light Based Over The Counter Wrinkle Reduction
- Decision date
- 2025-12-05
- Date received
- 2025-07-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K252142.pdf
Official FDA record: K252142
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.