meddevicedb.com FDA Device Reference

SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1

K250361 Class II Traditional
Decision Date
2025-05-23
Sponsor / Applicant
Geske Beauty Tech GmbH

Technical Specification

510(k) Submission ID K250361
Product Code NFO
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5890
Decision Date 2025-05-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 received FDA 510(k) clearance under submission number K250361, sponsored by Geske Beauty Tech GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2025-05-23.

Classification & Regulation

This clearance is catalogued under FDA product code NFO and 21 CFR 882.5890, within the Neurology review panel as a Class II device.