# Duoject Medical Systems, Inc.

- Location (FDA's records): Bromont, Qc., CA
- FDA decisions: 3 (2001–2014): 3 510(k) clearances
- Product codes: LHI (3)
- Predicates its devices cite: 5 (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
- West Pharmaceutical Services, Inc.: 2 (https://510kreport.com/company/west-pharmaceutical-services)
- Bioject, Inc.: 1 (https://510kreport.com/company/bioject)
- Bioject Medical Technologies, Inc.: 1 (https://510kreport.com/company/bioject-medical-technologies)

## Firms that cite its devices most
- Pharmc, LLC: 1 (https://510kreport.com/company/pharmc)
- West Pharmaceutical Services, Inc.: 1 (https://510kreport.com/company/west-pharmaceutical-services)

## Its most-cited devices
- K133097: E-Z Link (2014), cited by 1
- K070584: Smart-Rod (2008), cited by 1
- K010703: Inter-Vial (2001), cited by 1

## Recent decisions
- K133097: E-Z Link (Mar 13, 2014)
- K070584: Smart-Rod (Apr 2, 2008)
- K010703: Inter-Vial (Jun 25, 2001)

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