Class Class II
SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 (K250361)
Description
SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 by Geske Beauty Tech GmbH, an FDA 510(k) cleared neurology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK250361
Clearance Date2025-05-23
Clearance TypeTraditional
Product CodeNFO
Regulation Number882.5890
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K250361
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 (K250361) cites 3 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K221443 | PureLift Pro Plus | Xtreem Pulse, LLC | 2022 |
| K181008 | NuFACE Trinity | Carol Cole Company Dba Nuface | 2018 |
| K171588 | NuBODY Skin Toning Device | Carol Cole Company Dba Nuface | 2017 |
Trace the full predicate network for K250361
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.