K242151
- 510(k) number
- K242151
- Device name
- Radiant Renewal Skincare Wand (HD-44,HD-44A ,HD-44B,HD-44C, HD-69, HD-69A, HD-69B)
- Applicant
- Shenzhen Nuon Medical Equipment Co., Ltd. CN
- Product code
- OHS — Light Based Over The Counter Wrinkle Reduction
- Decision date
- 2025-04-08
- Date received
- 2024-07-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
510(k) Summary (official FDA PDF): K242151.pdf
Official FDA record: K242151
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.