# Endo GI Medical

- Location (FDA's records): Nazareth, IL
- FDA decisions: 2 (2020–2022): 2 510(k) clearances
- Product codes: FGE (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 3 (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
- Endogi Medical, Ltd.: 1 (https://510kreport.com/company/endogi-medical)

## Firms that cite its devices most
- Endogi Medical, Ltd.: 2 (https://510kreport.com/company/endogi-medical)

## Its most-cited devices
- K202477: EndoGI S-Path Biliary Stent System (2020), cited by 2
- K222627: EndoGI S-Path Biliary Stent System (2022), cited by 1

## Recent decisions
- K222627: EndoGI S-Path Biliary Stent System (Sep 28, 2022)
- K202477: EndoGI S-Path Biliary Stent System (Sep 24, 2020)

Source page: https://510kreport.com/company/endo-gi-medical