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FDA 510(k)

MF SC GEN2 Facial Toning System

K-Number: K252218 · 2025-07-18

ApplicantMicro Current Technology, Inc.
Decision Date2025-07-18
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MF SC GEN2 Facial Toning System is a medical device manufactured by Micro Current Technology, Inc.. It received FDA 510(k) clearance on 2025-07-18 under approval number K252218. 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 MF SC GEN2 Facial Toning System?

MF SC GEN2 Facial Toning System is a medical device that received FDA 510(k) clearance on 2025-07-18. It is manufactured by Micro Current Technology, Inc.. The 510(k) number is K252218.

When was MF SC GEN2 Facial Toning System approved by the FDA?

MF SC GEN2 Facial Toning System received FDA 510(k) clearance on 2025-07-18, under approval number K252218.

What company makes MF SC GEN2 Facial Toning System?

MF SC GEN2 Facial Toning System is manufactured by Micro Current Technology, Inc..

What is the FDA product code for MF SC GEN2 Facial Toning System?

The FDA product code for MF SC GEN2 Facial Toning System is NFO.

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Other Devices by Micro Current Technology, Inc.

K181062Ultra Facial Toning System K183189Ultra OTC Facial Toning System K233525MF SC Facial Toning System K233095S21 OTC Transcutaneous Electrical Nerve Stimulator

Related Devices (Code: 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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