# Neoguide Systems, Inc.

- Location (FDA's records): Los Gatos, CA
- FDA decisions: 2 (2006–2007): 2 510(k) clearances
- Product codes: FDF (2)
- Predicates its devices cite: 9 (1 its own); citations of its devices by later devices: 7 (1 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 Optical Co., Ltd.: 2 (https://510kreport.com/company/olympus-optical)
- Pentax Precision Instrument Corp.: 2 (https://510kreport.com/company/pentax-precision-instrument)
- Sightline Technologies, Ltd.: 2 (https://510kreport.com/company/sightline-technologies)
- Usgi Medical: 2 (https://510kreport.com/company/usgi-medical)

## Firms that cite its devices most
- Medrobotics Corporation: 3 (https://510kreport.com/company/medrobotics)
- Invendo Medical Gbmh: 2 (https://510kreport.com/company/invendo-medical-gbmh)
- Neptune Medical, Inc.: 1 (https://510kreport.com/company/neptune-medical)

## Its most-cited devices
- K070622: Neoguide Endoscopy System (2007), cited by 4
- K052930: Navigator Endoscopy System (2006), cited by 3

## Recent decisions
- K070622: Neoguide Endoscopy System (Aug 14, 2007)
- K052930: Navigator Endoscopy System (Jan 31, 2006)

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