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Inter Medical Medizintechnik GmbH

FDA Regulatory Profile

Inter Medical Medizintechnik GmbH has 0 FDA recalls, 1 inspection, 3 510(k) clearances and 0 compliance actions on record.

Latest inspection
Mar 16, 2023 · VAI
Latest 510(k)
Apr 13, 2023

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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) clearances3Oct 4, 2026Not statedCurrent
Inspections1Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Mar 16, 2023Lubbecke, GermanyDevicesVoluntary Action Indicated (VAI)3006611212

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
K230393UniCam Evo SoftwareApr 13, 2023
K132347MULTICAM 3000 ECONov 20, 2013
K052473CX 250 C PLUS WITH GAMMAXP SOFTWARE, MODEL 0121 0000Oct 28, 2005

FDA data resources