# Artiria Medical SA

- Location (FDA's records): Geneva, CH
- FDA decisions: 1 (2023–2023): 1 510(k) clearance
- Product codes: MOF (1)
- Predicates its devices cite: 2 (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
- Stryker Corp.: 1 (https://510kreport.com/company/stryker)
- Boston Scientific - Precision Vascular: 1 (https://510kreport.com/company/boston-scientific-precision-vascular)

## Recent decisions
- K222690: SmartGUIDE deflectable hydrophilic guidewire (Apr 24, 2023)

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