Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in IsraelLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Philips. FDA records under 5 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Philips Medical Systems Technologies with 5 510(k) clearances, 2 AI-enabled devices and 1 device recall. The most recent is a 510(k) clearance dated Mar 27, 2026: Spectral CT Verida Family.
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.
| Mar 27, 2026 | Spectral CT Verida FamilyK253649 · JAK | 510(k) clearances |
| Mar 27, 2026 | Spectral CT Verida FamilyK253649 · Radiology | AI-enabled devices |
| May 16, 2025 | Spectral CTK244008 · JAK | 510(k) clearances |
| Oct 18, 2024 | Spectral CT 7500 RTK240844 · JAK | 510(k) clearances |
| Oct 10, 2024 | Vue PACS Diagnostic Viewer with Vue PACS client 12.1.5 to 12.2.8.454 software Model Number: 1149418 Intended use is to provide completeClass II · A software issue affecting Philips Vue PACS may cause incorrect ischemic map and table value calculations when using the | Device recalls |
| Apr 24, 2024 | Image Management V15K240822 · LLZ | 510(k) clearances |
| Jan 12, 2018 | Illumeo SystemK173588 · LLZ | 510(k) clearances |
| Jan 12, 2018 | Illumeo SystemK173588 · Radiology | AI-enabled devices |
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
