Diagnostics 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 2 companies' records, each linked to the record.
As of Nov 15, 2026, FDA's public records list Circassia Pharmaceuticals and its 2 subsidiaries with 6 510(k) clearances. The most recent is a 510(k) clearance dated Nov 22, 2017: NIOX VERO.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Circassia Pharmaceuticals and its 2 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Nov 22, 2017 | NIOX VEROK170983 · MXA | 510(k) clearances |
| Feb 26, 2015 | NIOX VERO Airway Inflammation MonitorK150233 · MXA | 510(k) clearances |
| Nov 6, 2014 | NIOX VERO AIRWAY INFLAMMATION MONITORK133898 · MXA | 510(k) clearances |
| Dec 27, 2012 | NIOX PANEL FOR USE WITH THE NIOX MINO AIRWAY INFLAMMATION MONITORK123683 · MXA | 510(k) clearances |
| Sep 2, 2010 | NIOX MINO MODEL 09-1000K101034 · MXA | 510(k) clearances |
| Mar 3, 2008 | NIOX MINOK072816 · MXA | 510(k) clearances |
| Apr 30, 2003 | NIOX ARTICLE NO: 02-1000DEN030001 · MXA | 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
