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Siemens Medical Solution USA, Inc.

FDA Regulatory Profile

Siemens Medical Solution USA, Inc. has 0 FDA recalls, 0 inspections, 8 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Aug 16, 2022

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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) clearances8Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K220433syngo Application Software (VE21)Aug 16, 2022
K201156ARTIS pheno (VE2)Jun 29, 2020
K193178Biograph HorizonFeb 12, 2020
K190780syngo Application SoftwareSep 12, 2019
K190757MAGNETOM Avanto FitMay 31, 2019
K181407Artis zee/zeego & Artis Q/Q.zenAug 15, 2018
K163286ARTIS phenoMar 9, 2017
K163285syngo Application SoftwareFeb 14, 2017

FDA data resources