meddevicedb.com FDA Device Reference

GLAM LED Facial Mask (TB-2386F)

K251727 Class II Traditional
Decision Date
2025-08-29
Sponsor / Applicant
Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.

Technical Specification

510(k) Submission ID K251727
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2025-08-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GLAM LED Facial Mask (TB-2386F) received FDA 510(k) clearance under submission number K251727, sponsored by Touchbeauty Beauty & Health (Shenzhen) 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 2025-08-29.

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.