Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Micro Current Technology, Inc. — Predicate Candidate Screening
8 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
23 daysmedian FDA review time
157 days90th percentile
8clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K252218 | MF SC GEN2 Facial Toning System | Micro Current Technology, Inc. | 2025-07-18 | 3 | 0 |
| K233095 | S21 OTC Transcutaneous Electrical Nerve Stimulator | Micro Current Technology, Inc. | 2024-03-01 | 157 | 0 |
| K233525 | MF SC Facial Toning System | Micro Current Technology, Inc. | 2023-11-24 | 23 | 0 |
| K183189 | Ultra OTC Facial Toning System | Micro Current Technology, Inc. | 2019-04-17 | 149 | 0 |
| K181062 | Ultra Facial Toning System | Micro Current Technology, Inc. | 2018-07-18 | 86 | 0 |
| K033253 | S21 TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR | Micro Current Technology, Inc. | 2003-10-21 | 13 | 0 |
| K032653 | E275 | Micro Current Technology, Inc. | 2003-09-12 | 15 | 0 |
| K993823 | MED-4000 | Micro Current Technology, Inc. | 1999-11-19 | 7 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda