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FDA 510(k)

SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1

K-Number: K250361 · 2025-05-23

ApplicantGeske Beauty Tech GmbH
Decision Date2025-05-23
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 is a medical device manufactured by Geske Beauty Tech GmbH. It received FDA 510(k) clearance on 2025-05-23 under approval number K250361. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1?

SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 is a medical device that received FDA 510(k) clearance on 2025-05-23. It is manufactured by Geske Beauty Tech GmbH. The 510(k) number is K250361.

When was SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 approved by the FDA?

SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 received FDA 510(k) clearance on 2025-05-23, under approval number K250361.

What company makes SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1?

SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 is manufactured by Geske Beauty Tech GmbH.

What is the FDA product code for SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1?

The FDA product code for SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 is NFO.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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