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Micro Medical Solutions, Inc.

FDA Regulatory Profile

Micro Medical Solutions, Inc. has 0 FDA recalls, 3 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 2, 2025 · VAI
Latest 510(k)
Apr 25, 2016

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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) clearances2Nov 8, 2026File dated Nov 2, 2026Current
Inspections3Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 2, 2025Woburn, MADevicesVoluntary Action Indicated (VAI)3013391155
May 23, 2025Woburn, MADevicesVoluntary Action Indicated (VAI)3013391155
Jan 15, 2020Woburn, MADevicesNo Action Indicated (NAI)3013391155

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3013391155Woburn, MA3Jul 2, 2025

Recent 510(k) Clearances

K-NumberDeviceDate
K152934MMS PTA Balloon CatheterApr 25, 2016
K152625MMS Guide CatheterMar 9, 2016

FDA data resources

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