Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in CanadaLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of StrykerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 4 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Novadaq Technologies with 15 510(k) clearances and 7 device recalls. The most recent is a 510(k) clearance dated Jan 11, 2017: SPY Phi Open Field Handheld Fluorescence Imaging 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.
| Jan 11, 2017 | SPY Phi Open Field Handheld Fluorescence Imaging SystemK162885 · OWN | 510(k) clearances |
| Sep 20, 2016 | PINPOINT Endoscopic Fluorescence Imaging SystemK161792 · GCJ | 510(k) clearances |
| May 23, 2016 | PINPOINT Endoscopic Fluorescence Imaging SystemK150956 · GCJ | 510(k) clearances |
| Jan 29, 2016 | PINPOINT Endoscopic Fluorescence Imaging SystemClass II · It has been determined that the PINPOINT Operator's Manual does not contain validated parameters for gravity-cycle autoc | Device recalls |
| Mar 22, 2013 | ENDOSCOPIC INTRODUCERK123013 · FED | 510(k) clearances |
| Feb 4, 2011 | SPY INTRA-OPERATIVE IMAGING SYSTEMK100371 · IZI | 510(k) clearances |
| Jul 9, 2009 | SPY SCOPE INTRA-OPERATIVE OPERATING SYSTEMK091515 · GCJ | 510(k) clearances |
| Sep 17, 2008 | SPY ANALYSIS TOOLKIT, MODEL SA9000K081792 · LLZ | 510(k) clearances |
| Jan 10, 2008 | SPY FLUORESCENT IMAGING SYSTEMK073088 · IZI | 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
