# Bioject Medical Technologies, Inc.

- Location (FDA's records): Bedminster, NJ
- FDA decisions: 3 (2004–2012): 3 510(k) clearances
- Product codes: LHI (2), KZE (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 2 (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
- Bioject, Inc.: 3 (https://510kreport.com/company/bioject)
- Bd Becton Dickinson Vacutainer Systems Preanalytic: 1 (https://510kreport.com/company/bd-becton-dickinson-vacutainer-systems-preanalytic)
- Terumo America, Inc.: 1 (https://510kreport.com/company/terumo-america)
- Pharmajet, Inc.: 1 (https://510kreport.com/company/pharmajet)

## Firms that cite its devices most
- Medimop Medical Projects, Ltd.: 1 (https://510kreport.com/company/medimop-medical-projects)
- Duoject Medical Systems, Inc.: 1 (https://510kreport.com/company/duoject-medical-systems)

## Its most-cited devices
- K043304: Q-Cap Needle-Free Reconstitution 13MM Vial Adapter, Model 6100-01 (2005), cited by 2

## Recent decisions
- K121270: Bioject Needle-Free Injection Management System (Jul 19, 2012)
- K043304: Q-Cap Needle-Free Reconstitution 13MM Vial Adapter, Model 6100-01 (Jan 14, 2005)
- K041564: Q-Cap Needle-Free Reconstitution 13MM Vial Adapter, Model 6100-01 (Jul 16, 2004)

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