# Medtronic Core Valve, LLC

- Location (FDA's records): Santa Rosa, CA
- FDA decisions: 2 (2015–2018): 2 510(k) clearances
- Product codes: DQX (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
- Medtronic, Inc.: 1 (https://510kreport.com/company/medtronic)

## Firms that cite its devices most
- Vascular Solutions, Inc.: 1 (https://510kreport.com/company/vascular-solutions)
- Medtronic, Inc.: 1 (https://510kreport.com/company/medtronic)

## Its most-cited devices
- K181001: Medtronic Confida Brecker Guidewire (2018), cited by 2
- K150465: Medtronic Confida Brecker Guidewire (2015), cited by 1

## Recent decisions
- K181001: Medtronic Confida Brecker Guidewire (May 3, 2018)
- K150465: Medtronic Confida Brecker Guidewire (Aug 3, 2015)

Source page: https://510kreport.com/company/medtronic-core-valve