# Guidant Endovascular Solutions, Inc.

- Location (FDA's records): Santa Clara, CA
- FDA decisions: 1 (2006–2006): 1 510(k) clearance
- Product codes: FGE (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 0 (0 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
- Guidant Corp.: 3 (https://510kreport.com/company/guidant)

## Recent decisions
- K060817: Omnilink. 018 Biliary Stent System (Jun 15, 2006)

Source page: https://510kreport.com/company/guidant-endovascular-solutions