FDA applicant
Micro Current Technology, Inc.
FDA records 8 decisions for Micro Current Technology, Inc. (Seattle, WA) from 1999 to 2025: 8 510(k) clearances. Most are in product codes NFO (Stimulator, Transcutaneous Electrical…) and GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). Since 2016 its 510(k)s took a median of 86 days from receipt to decision, against 128 for FDA’s reviews in the same codes and years. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Micro Current Technology, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Micro Current Technology, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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