# Duopross Meditech Corporation

- Location (FDA's records): Albuquerque, NM
- FDA decisions: 2 (2005–2005): 2 510(k) clearances
- Product codes: FMI (1), FMF (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
- M.K. Meditech Co., Ltd.: 4 (https://510kreport.com/company/mk-meditech)
- Terumo America, Inc.: 1 (https://510kreport.com/company/terumo-america)
- Bd Becton Dickinson Vacutainer Systems Preanalytic: 1 (https://510kreport.com/company/bd-becton-dickinson-vacutainer-systems-preanalytic)

## Firms that cite its devices most
- Sol-Milennium Medical, Inc.: 1 (https://510kreport.com/company/sol-milennium-medical)
- Wenzhou Wuzhou Group Co., Ltd.: 1 (https://510kreport.com/company/wenzhou-wuzhou-group)

## Its most-cited devices
- K052445: Duopross Needle (2005), cited by 1
- K042500: Duopross Syringes (2005), cited by 1

## Recent decisions
- K052445: Duopross Needle (Dec 5, 2005)
- K042500: Duopross Syringes (Feb 22, 2005)

Source page: https://510kreport.com/company/duopross-meditech