meddevicedb.com FDA Device Reference

808nm semiconductor laser hair removal machine

K252048 Class II Traditional
Decision Date
2026-02-03
Sponsor / Applicant
Xi'An Taibo Electronic Technology Co., Ltd.

Technical Specification

510(k) Submission ID K252048
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2026-02-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

808nm semiconductor laser hair removal machine received FDA 510(k) clearance under submission number K252048, sponsored by Xi'An Taibo Electronic Technology 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 2026-02-03.

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.