Medical Device Manufacturer · US , Albuquerque , NM

Duopross Meditech Corporation - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2005

Recent clearances: DUOPROSS NEEDLE, DUOPROSS SYRINGES

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Duopross Meditech Corporation General Hospital ✕

2 devices

1-2 of 2

Cleared Dec 05, 2005

DUOPROSS NEEDLE

General Hospital · 89d

Cleared Feb 22, 2005

DUOPROSS SYRINGES

General Hospital · 161d

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 25, 2026