Micro Current Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Micro Current Technology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MF SC GEN2 Facial Toning System, S21 OTC Transcutaneous Electrical Nerve Stimulator, MF SC Facial Toning System
8
Total
8
Cleared
0
Denied
Micro Current Technology, Inc. has 8 FDA 510(k) cleared medical devices. Based in Seattle, US.
Latest FDA clearance: Jul 2025. Active since 1999. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Micro Current Technology, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Regulatory Insight, Inc. and Regulatory Technology Services, LLC.
FDA 510(k) Regulatory Record - Micro Current Technology, Inc.
8 devices
Cleared
Jul 18, 2025
MF SC GEN2 Facial Toning System
Neurology
3d
Cleared
Mar 01, 2024
S21 OTC Transcutaneous Electrical Nerve Stimulator
Neurology
157d
Cleared
Nov 24, 2023
MF SC Facial Toning System
Neurology
23d
Cleared
Apr 17, 2019
Ultra OTC Facial Toning System
Physical Medicine
149d
Cleared
Jul 18, 2018
Ultra Facial Toning System
Neurology
86d
Cleared
Oct 21, 2003
S21 TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR
Neurology
13d
Cleared
Sep 12, 2003
E275
Neurology
15d
Cleared
Nov 19, 1999
MED-4000
Neurology
7d