# Orqis Medical Corporation

- Location (FDA's records): Lake Forest, CA
- FDA decisions: 1 (2008–2008): 1 510(k) clearance
- Product codes: KFM (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
- Levitronix, LLC: 1 (https://510kreport.com/company/levitronix)
- Cardiacassist, Inc.: 1 (https://510kreport.com/company/cardiacassist)
- Terumo Cardiovascular Systems Corp.: 1 (https://510kreport.com/company/terumo-cardiovascular-systems)

## Recent decisions
- K073631: Orqis Extracorporeal Blood Pumping System, Model BPS-100 (Jun 27, 2008)

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