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Microcurrent Research, Inc.

FDA Regulatory Profile

Microcurrent Research, Inc. has 0 FDA recalls, 0 inspections, 4 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Nov 25, 1998

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances4Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent 510(k) Clearances

K-NumberDeviceDate
K981976ACUTRON MENTOR MODEL 961Nov 25, 1998
K901902ACUSOURCE 600 FOR USE WITH TMJ ELECTRODEOct 9, 1990
K895977ACUSOURCE 600 (TENS)Jan 9, 1990
K890143ACUTRON MULTIWAVE FOR USE IN TMJ SYNDROME PAIN CONMay 1, 1989

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.