510(k) Report

FDA applicant

Duopross Meditech Corporation

Albuquerque, NM2 decisions2005–20050 recalls

FDA records 2 decisions for Duopross Meditech Corporation (Albuquerque, NM) in 2005: 2 510(k) clearances. Most are in product codes FMI (Needle, Hypodermic, Single Lumen) and FMF (Syringe, Piston). Its devices cite 6 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Duopross Meditech Corporation’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Duopross Meditech Corporation since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Duopross Meditech Corporation by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Duopross Meditech Corporation’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • FMINeedle, Hypodermic, Single Lumen1decision
  • FMFSyringe, Piston1decision

Whose devices does it build on?

Its devices cite 6 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K052445Duopross NeedleDuopross Meditech Corporation · 20051cites it
  • K042500Duopross SyringesDuopross Meditech Corporation · 20051cites it

What has FDA decided for it lately?

  • K052445Duopross NeedleDuopross Meditech Corporation · 2005
  • K042500Duopross SyringesDuopross Meditech Corporation · 2005

All 2 as Duopross Meditech Corporation →

Other applicant names beginning “Duopross”

FDA records each applicant name separately; these may or may not be the same firm.

Duopross Meditech Corporate 1