meddevicedb.com FDA Device Reference

LED Beauty Mask (RLBXX)

K252308 Class II Traditional
Decision Date
2025-11-13
Sponsor / Applicant
Atop Lighting Co., Ltd.

Technical Specification

510(k) Submission ID K252308
Product Code OHS
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2025-11-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LED Beauty Mask (RLBXX) received FDA 510(k) clearance under submission number K252308, sponsored by Atop Lighting 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 2025-11-13.

Classification & Regulation

This clearance is catalogued under FDA product code OHS and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.