510(k) Report

FDA applicant

Prodimed

Ringoes, NJ1 decision1999–19990 recalls

FDA records 1 decision for Prodimed (Ringoes, NJ) in 1999: 1 510(k) clearance. All are in product code MQH (Microtools, Assisted Reproduction (Pipettes)). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Prodimed since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • MQHMicrotools, Assisted Reproduction (Pipettes)1decision

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K983713Prodimed Microinjection PipettesProdimed · 19991cites it

What has FDA decided for it lately?

  • K983713Prodimed Microinjection PipettesProdimed · 1999

The one decision as Prodimed →