# Crux Biomedical

- Location (FDA's records): Menlo Park, CA
- FDA decisions: 2 (2012–2013): 2 510(k) clearances
- Product codes: DTK (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 2 (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
- Rex Medical: 1 (https://510kreport.com/company/rex-medical)

## Firms that cite its devices most
- Volcano Corporation: 1 (https://510kreport.com/company/volcano)

## Its most-cited devices
- K122585: Crux Vena Cava Filter System (2013), cited by 1
- K120402: Crux Vena Cava Filter System (2012), cited by 1

## Recent decisions
- K122585: Crux Vena Cava Filter System (Jan 17, 2013)
- K120402: Crux Vena Cava Filter System (Jul 13, 2012)

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