# Via Biomedical, Inc.

- Location (FDA's records): Maple Grove, MN
- FDA decisions: 1 (2009–2009): 1 510(k) clearance
- Product codes: DQY (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 2 (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
- Medtronic Endovascular Innovations: 1 (https://510kreport.com/company/medtronic-endovascular-innovations)
- Cook, Inc.: 1 (https://510kreport.com/company/cook)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)

## Firms that cite its devices most
- Arch Catheter, LLC: 1 (https://510kreport.com/company/arch-catheter)
- Qxmedical, LLC: 1 (https://510kreport.com/company/qxmedical)

## Its most-cited devices
- K091624: Stent Graft Balloon Catheter (2009), cited by 2

## Recent decisions
- K091624: Stent Graft Balloon Catheter (Oct 15, 2009)

Source page: https://510kreport.com/company/via-biomedical