# Avantis Medical Systems, Inc.

- Location (FDA's records): Sunnyvale, CA
- FDA decisions: 6 (2007–2016): 6 510(k) clearances
- Product codes: FDF (6)
- Predicates its devices cite: 12 (8 its own); citations of its devices by later devices: 10 (8 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Olympus Opto-Electronics Co., Ltd.: 1 (https://510kreport.com/company/olympus-opto-electronics)
- Olympus Corp.: 1 (https://510kreport.com/company/olympus)
- United States Endoscopy Group, Inc.: 1 (https://510kreport.com/company/united-states-endoscopy-group)
- Olympus America, Inc.: 1 (https://510kreport.com/company/olympus-america)

## Firms that cite its devices most
- Visura Technologies, LLC: 1 (https://510kreport.com/company/visura-technologies)
- Invendo Medical Gbmh: 1 (https://510kreport.com/company/invendo-medical-gbmh)

## Its most-cited devices
- K070330: Third Eye Retroscope Auxiliary Endoscopy System (2007), cited by 3
- K091783: Third Eye Retroscope Auxiliary Endoscope System (2009), cited by 2
- K083180: Third Eye Retroscope Auxiliary Endoscopy System (2009), cited by 2
- K140595: Third Eye Panoramic Auxiliary Endoscopy System (2014), cited by 2
- K093187: Modification to Third Eye Retroscope Auxiliary Endoscopy System (2009), cited by 1

## Recent decisions
- K160356: Third Eye Panoramic Auxiliary Endoscopy System - Resposable (May 17, 2016)
- K140595: Third Eye Panoramic Auxiliary Endoscopy System (Nov 17, 2014)
- K093187: Modification to Third Eye Retroscope Auxiliary Endoscopy System (Nov 5, 2009)
- K091783: Third Eye Retroscope Auxiliary Endoscope System (Jul 7, 2009)
- K083180: Third Eye Retroscope Auxiliary Endoscopy System (Feb 12, 2009)
- K070330: Third Eye Retroscope Auxiliary Endoscopy System (Apr 24, 2007)

Source page: https://510kreport.com/company/avantis-medical-systems