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As of Nov 15, 2026, FDA's public records list Toshibamedical Systems Corporation with 80 510(k) clearances. The most recent is a 510(k) clearance dated Apr 20, 2018: Viamo c100 TUS-VC100 Diagnostic Ultrasound System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Apr 20, 2018 | Viamo c100 TUS-VC100 Diagnostic Ultrasound SystemK173962 · IYN | 510(k) clearances |
| Feb 23, 2018 | Aquilion Precision (TSX-304A/2) V8.6 with FIRST 3.0K173468 · JAK | 510(k) clearances |
| Jan 31, 2018 | Vitrea Software Toshiba Package VSTP-001AK173088 · LLZ | 510(k) clearances |
| Jan 26, 2018 | Vantage Galan 3T, V4.6K173382 · LNH | 510(k) clearances |
| Jan 11, 2018 | Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, V2.4K173090 · IYN | 510(k) clearances |
| Dec 14, 2017 | Infinix-i, INFX-8000V, V7.0K172863 · OWB | 510(k) clearances |
| Dec 12, 2017 | Xario 200 Diagnostic Ultrasound System V6.0K172276 · IYN | 510(k) clearances |
| Oct 30, 2017 | XIDF-AWS801, Angio Workstation, V7.0K172646 · OWB | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
