Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Avantis Medical Systems with 6 510(k) clearances. The most recent is a 510(k) clearance dated May 17, 2016: Third Eye Panoramic Auxiliary Endoscopy System - Resposable.
| May 17, 2016 | Third Eye Panoramic Auxiliary Endoscopy System - ResposableK160356 · FDF | 510(k) clearances |
| Nov 17, 2014 | THIRD EYE PANORAMIC AUXILIARY ENDOSCOPY SYSTEMK140595 · FDF | 510(k) clearances |
| Nov 5, 2009 | MODIFICATION TO THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPY SYSTEMK093187 · FDF | 510(k) clearances |
| Jul 7, 2009 | THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPE SYSTEMK091783 · FDF | 510(k) clearances |
| Feb 12, 2009 | THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPY SYSTEMK083180 · FDF | 510(k) clearances |
| Apr 24, 2007 | THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPY SYSTEMK070330 · FDF | 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
