# Injectimed, Inc.

- Location (FDA's records): Albuquerque, NM
- FDA decisions: 3 (1992–2008): 3 510(k) clearances
- Product codes: MDM (1), DYB (1), FMI (1)
- Predicates its devices cite: 8 (1 its own); citations of its devices by later devices: 1 (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
- Medamicus, Inc.: 3 (https://510kreport.com/company/medamicus)
- Minrad, Inc.: 1 (https://510kreport.com/company/minrad)
- Ocean Medical Products, Ltd.: 1 (https://510kreport.com/company/ocean-medical-products)
- Manan Manufacturing Co., Inc.: 1 (https://510kreport.com/company/manan-manufacturing)
- Needle Tech Products, Inc.: 1 (https://510kreport.com/company/needle-tech-products)

## Its most-cited devices
- K040029: Safetynet Guidewire Introducer (2004), cited by 1

## Recent decisions
- K073664: Frontline Medical Safetynet Guidewire Introducer (Aug 8, 2008)
- K040029: Safetynet Guidewire Introducer (Apr 5, 2004)
- K922158: Protector Syringe Safety Cap System (Jul 21, 1992)

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