K260202
- 510(k) number
- K260202
- Device name
- LED Light Therapy Masks (LumiLips FAC07NA)
- Applicant
- Guangdong Newdermo Biotech Co., Ltd. CN
- Product code
- OHS — Light Based Over The Counter Wrinkle Reduction
- Decision date
- 2026-03-23
- Date received
- 2026-01-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
510(k) Summary (official FDA PDF): K260202.pdf
Official FDA record: K260202
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.