Imagine Milling Technologies, LLC

FDA Regulatory Profile

Imagine Milling Technologies, LLC has 0 FDA recalls, 3 inspections, 4 510(k) clearances and 0 compliance actions on record.

Latest inspection
Feb 1, 2023 · VAI
Latest 510(k)
Jun 27, 2026

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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
Inspections3Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Feb 1, 2023Milford, NHDevicesVoluntary Action Indicated (VAI)3009727738
Jul 26, 2018Milford, NHDevicesVoluntary Action Indicated (VAI)3009727738
Nov 22, 2017Milford, NHDevicesNo Action Indicated (NAI)3009727738

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 3009727738Milford, NH3Feb 1, 2023

Recent 510(k) Clearances

K-NumberDeviceDate
K261122MIST ICJun 27, 2026
K243009MIST ICJun 24, 2025
K222368MIST ICDec 1, 2022
K182246MIST ICApr 16, 2019

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