SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1— 510(k) K250361

Name: FDA 510(k) clearance K250361
Creator: U.S. Food and Drug Administration
Published: 2025-05-23

Substantially Equivalent

Geske Beauty Tech GmbH

FDA 510(k) clearance K250361 for SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1, Substantially Equivalent on 2025-05-23. Applicant: Geske Beauty Tech GmbH. Device class: 2.

Clearance details

Applicant: Geske Beauty Tech GmbH
Product code: Code NFO
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2025-02-10
Decision date: 2025-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Berlin, DE

Download summary PDF View on FDA.gov ↗

Recent devices under product code NFO

view all

K262861 — PureLift Pro Max2026-09-11
K260387 — SYNERJET PRO (SP-1003); InPhiuse (SP-1003); WOWJET (SP-1003)2026-08-31
K253932 — FACEGYM Pro Device (HD-109)2026-07-23
K260179 — VITA Multi-Function Head Brush (TB-2343F, TB-2442F)2026-06-03
K260895 — Ulike Clear Zero (YC10 BU)2026-05-28

Data sourced from openFDA. This site is unofficial and independent of the FDA.