# Endogi Medical, Ltd.

- Location (FDA's records): Nazareth, IL
- FDA decisions: 2 (2020–2023): 2 510(k) clearances
- Product codes: FGE (2)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 2 (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
- Endo GI Medical: 2 (https://510kreport.com/company/endo-gi-medical)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)

## Firms that cite its devices most
- Endo GI Medical: 1 (https://510kreport.com/company/endo-gi-medical)

## Its most-cited devices
- K193600: EndoGI Biliary Stent System (2020), cited by 2

## Recent decisions
- K232596: EndoGI S-Path Biliary Stent System (Sep 27, 2023)
- K193600: EndoGI Biliary Stent System (Jun 26, 2020)

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