SimBioSys, Inc. is one of 16101 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
SimBioSys, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TumorSight Risk, TumorSight Viz, TumorSight Viz
4
Total
4
Cleared
0
Denied
SimBioSys, Inc. has 4 FDA 510(k) cleared medical devices. Based in Chicago, US.
Latest FDA clearance: Sep 2026. Active since 2023. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by SimBioSys, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Hogan & Lovells U.S. Lpp and Hogan Lovells US LLP.
FDA 510(k) Regulatory Record - SimBioSys, Inc.
4 devices