Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA files no records under this name; these are its 3 companies' records, each linked to the record.
As of Nov 13, 2026, FDA's public records list Neusoft Corporation and its 3 subsidiaries with 5 510(k) clearances and 1 device recall. The most recent is a device recall dated Jan 9, 2019: NeuViz 128 Multi-slice CT Scanner System with software version 1.0.8.5010O+P04 Vi .0.8.….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Neusoft Corporation and its 3 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Jan 9, 2019 | NeuViz 128 Multi-slice CT Scanner System with software version 1.0.8.5010O+P04 Vi .0.8.521 9+PO1 Multi-Slice CT Scanner System can be usedClass II · For surview scan length more than 500mm,if the user aborts or skips the reconstructed surview, the image may have the wr | Device recalls |
| Apr 24, 2009 | ATTRIUS, MODEL PET150A6001, ATTRIUS L, MODEL PET150A8001, TRUESIGHT, MODEL NSP-P6C, TRUESIGHT, MODEL NSP-P8K090178 · KPS | 510(k) clearances |
| Jun 17, 2004 | CT-C3000DUAL AND CT-C2800DUAL FAMILY OF DUAL-SLICE CT SCANNER SYSTEMSK041542 · JAK | 510(k) clearances |
| Oct 29, 2003 | SUPEROPEN 0.23T, MODEL NAM-P023AK033315 · LNH | 510(k) clearances |
| Apr 1, 2003 | SUPEROPEN 0.35T, MODEL NSM-P035K030918 · LNH | 510(k) clearances |
| Apr 3, 2002 | CT-C3000 SPIRAL CT SCANNER SYSTEMK020913 · JAK | 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
