meddevicedb.com FDA Device Reference

Advanced Cryo Skin Tag Remover (Advanced Skin Tag Remover)

K252198 Class II Traditional
Decision Date
2026-04-02
Sponsor / Applicant
Medical Brands Laboratories B.V.

Technical Specification

510(k) Submission ID K252198
Product Code GEH
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4350
Decision Date 2026-04-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Advanced Cryo Skin Tag Remover (Advanced Skin Tag Remover) received FDA 510(k) clearance under submission number K252198, sponsored by Medical Brands Laboratories B.V.. 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 2026-04-02.

Classification & Regulation

This clearance is catalogued under FDA product code GEH and 21 CFR 878.4350, within the General, Plastic Surgery review panel as a Class II device.