The Healthcare AI Institute / Transparency Registry
Transparency Registry · applicant

Siemens Medical Solutions USA, Inc.: 17 FDA AI clearances

Every 510(k) clearance held by Siemens Medical Solutions USA, Inc. under the AI-associated product codes this registry tracks, from openFDA public records, refreshed weekly. Facts only; listing is not evaluation.

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DeviceDecision dateCategory
syngo.CT Coronary Cockpit2026-06-25QIH
syngo Application Software2026-04-29QIH
MI View&GO2026-02-10QIH
syngo.via MI Workflows; Scenium; syngo MBF2025-07-03QIH
syngo.CT LVO Detection2025-04-10QAS
MI View&GO2024-08-30QIH
syngo.via MI Workflows; Scenium; syngo MBF2024-08-30QIH
syngo.CT Brain Hemorrhage2024-03-22QAS
syngo.via MI Workflows; Scenium; syngo MBF2023-11-28QIH
Syngo Dynamics (Version VA40F)2022-11-14QIH
AI-Rad Companion Organs RT2022-10-14QKB
MI View&GO2022-08-19QIH
syngo.CT Brain Hemorrhage2022-01-28QAS
syngo.via MI WorkFlows, Scenium, syngo MBF2021-06-10QIH
syngo.via MI Workflows, syngo MBF2020-11-18QIH
AI-Rad Companion Organs RT2020-11-06QKB
AI-Rad Companion Prostate MR2020-07-30QIH

Sources linked on each entry. Coverage note: this lists clearances under tracked AI-associated codes only — the company may hold other clearances outside them. Work for Siemens Medical Solutions USA, Inc.? The disclosure rows on your entries update free on submission of public links — start here.

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