# Ostial Solutions, LLC

- Location (FDA's records): Sunnyvale, CA
- FDA decisions: 1 (2007–2007): 1 510(k) clearance
- Product codes: DQX (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 4 (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
- Cordis Corp.: 1 (https://510kreport.com/company/cordis)
- Lake Region Mfg., Inc.: 1 (https://510kreport.com/company/lake-region-mfg)
- Ev3, Inc.: 1 (https://510kreport.com/company/ev3)
- Biosphere Medical, S.A.: 1 (https://510kreport.com/company/biosphere-medical)

## Firms that cite its devices most
- Merit Medical Systems, Inc.: 1 (https://510kreport.com/company/merit-medical-systems)
- Shepherd Scientific, Inc.: 1 (https://510kreport.com/company/shepherd-scientific)
- Paieon, Inc.: 1 (https://510kreport.com/company/paieon)
- Medivalve, Ltd.: 1 (https://510kreport.com/company/medivalve)

## Its most-cited devices
- K062192: Ostial Pro Stent Positioning System (2007), cited by 4

## Recent decisions
- K062192: Ostial Pro Stent Positioning System (May 24, 2007)

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