Clearance Summary
LumiGlam Laser System (SHE-LSP601-3) received FDA 510(k) clearance under submission number K260690, sponsored by Beijing Sano Laser S&T Development Co.,Ltd. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2026-06-04.
- Submission: K260690
- Applicant / Sponsor: Beijing Sano Laser S&T Development Co.,Ltd
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2026-06-04
Classification & Regulation
This clearance is catalogued under FDA product code GEX and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.