meddevicedb.com FDA Device Reference

Wrinkle Retreat Pro Light Therapy Face Mask (Model: PH-m03)

K252983 Class II Traditional
Decision Date
2025-12-17
Sponsor / Applicant
Shenzhen Goodwind Technology Development Co., Ltd.

Technical Specification

510(k) Submission ID K252983
Product Code OHS
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2025-12-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Wrinkle Retreat Pro Light Therapy Face Mask (Model: PH-m03) received FDA 510(k) clearance under submission number K252983, sponsored by Shenzhen Goodwind Technology 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 2025-12-17.

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.