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Insert Molding Solutions, Inc.

FDA Regulatory Profile

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

Latest inspection
Aug 7, 2026 · NAI
Latest 510(k)
Mar 26, 2018

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances2Oct 4, 2026Not statedCurrent
Inspections3Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 7, 2026Cumming, GADevicesNo Action Indicated (NAI)3009050824
Jun 28, 2018Cumming, GADevicesNo Action Indicated (NAI)3009050824
May 6, 2016Cumming, GADevicesNo Action Indicated (NAI)3009050824

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.

Recent 510(k) Clearances

K-NumberDeviceDate
K172760REST EAZY ApplianceMar 26, 2018
K111529MAGNUM CORE TISSUE BIOPSY NEEDLE MODEL MN1820, RP CUTTING NEEDLE MODEL RP-1820, MCN CORE TISSUE…Jul 29, 2011

FDA data resources