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FDA 510(k)

MF SC GEN2 Facial Toning System

K-Number: K252218 · 2025-07-18

Decision Date2025-07-18
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MF SC GEN2 Facial Toning System is the device name listed in this FDA 510(k) record. The listed applicant is Micro Current Technology, Inc.. It received FDA 510(k) clearance on 2025-07-18 under 510(k) 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. The listed applicant is Micro Current Technology, Inc.. The 510(k) number is K252218.

When did MF SC GEN2 Facial Toning System receive FDA 510(k) clearance?

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

Who is the listed applicant for MF SC GEN2 Facial Toning System?

The FDA 510(k) record lists Micro Current Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Micro Current Technology, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: NFO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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