# Innoject, Inc.

- Location (FDA's records): Washington, DC
- FDA decisions: 1 (2004–2004): 1 510(k) clearance
- Product codes: KZH (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 1 (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
- Owen Mumford USA, Inc.: 2 (https://510kreport.com/company/owen-mumford-usa)
- Bd Becton Dickinson Vacutainer Systems Preanalytic: 1 (https://510kreport.com/company/bd-becton-dickinson-vacutainer-systems-preanalytic)
- Scandinavian Health Limited: 1 (https://510kreport.com/company/scandinavian-health)

## Firms that cite its devices most
- Pharma-Pen, Inc.: 1 (https://510kreport.com/company/pharma-pen)

## Its most-cited devices
- K042557: Innoject Auto-Injector (2004), cited by 1

## Recent decisions
- K042557: Innoject Auto-Injector (Nov 8, 2004)

Source page: https://510kreport.com/company/innoject