Data / Medical devices / United States / Micro Current Technology, Inc.

Micro Current Technology, Inc.: FDA-registered device maker in Seattle, WA, United States, 8 510(k) clearances

Name: Micro Current Technology, Inc. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Micro Current Technology, Inc. is registered with the FDA (registration 3026264) in Seattle, WA, United States. It lists 6 device types. The FDA files 8 510(k) clearances under its listings, the newest dated July 18, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3026264
FEI number: 1000126561
Address: 2244 1st Ave S, Seattle, WA, United States, 98134
Owner or operator: MICRO CURRENT TECHNOLOGY, INC. (9003838)
Roles: Manufacturer, Repackager or relabeler
First device listed: August 27, 2003
Registered through: 2026
Brand names listed: AUTO CARE, BIO-BRASION, BIO-DERMOLOGY, Bio-Ultimate Platinum, CUSTOM CARE, HOME CARE, MED 275, PAIN CARE and more

Devices it lists

Device	Product code	Class	Role	Source
Continuous Measurement Thermometer	FLL	2	Repackager or relabeler	accessdata.fda.gov
Dermatome	GFD	1	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Massager, Therapeutic, Electric	ISA	1	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Stimulator, Nerve, Transcutaneous, For Pain Relief	GZJ	2	Manufacturer	accessdata.fda.gov
Stimulator, Nerve, Transcutaneous, Over-The-Counter	NUH	2	Manufacturer	accessdata.fda.gov
Stimulator, Transcutaneous Electrical, Aesthetic Purposes	NFO	2	Manufacturer, Repackager or relabeler	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
July 18, 2025	K252218	MF SC GEN2 Facial Toning System	NFO	Substantially Equivalent	Micro Current Technology, Inc.	accessdata.fda.gov
March 1, 2024	K233095	S21 OTC Transcutaneous Electrical Nerve Stimulator	NUH	Substantially Equivalent	Micro Current Technology, Inc.	accessdata.fda.gov
November 24, 2023	K233525	MF SC Facial Toning System	NFO	Substantially Equivalent	Micro Current Technology, Inc.	accessdata.fda.gov
April 17, 2019	K183189	Ultra OTC Facial Toning System	NFO	Substantially Equivalent	Micro Current Technology, Inc.	accessdata.fda.gov
April 3, 2019	K182597	Infrared thermometer	FLL	Substantially Equivalent	Shenzhen Pango Electronic Co., Ltd.	accessdata.fda.gov
July 18, 2018	K181062	Ultra Facial Toning System	NFO	Substantially Equivalent	Micro Current Technology, Inc.	accessdata.fda.gov
October 21, 2003	K033253	S21 TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR	GZJ	Substantially Equivalent	Micro Current Technology, Inc.	accessdata.fda.gov
September 12, 2003	K032653	E275	GZJ	Substantially Equivalent	Micro Current Technology, Inc.	accessdata.fda.gov

Compare with other makers

Updated July 18, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.