510(k) Report

FDA applicant

Duomed, Inc.

West Palm Beach, FL1 decision2003–20030 recalls

FDA records 1 decision for Duomed, Inc. (West Palm Beach, FL) in 2003: 1 510(k) clearance. All are in product code GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). Its devices cite 2 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Duomed, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Which product codes does it file in?

  • GZJStimulator, Nerve, Transcutaneous, For Pain Relief1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K030140Duomed, Series 500, (Models ID 500, FL 500)Duomed, Inc. · 2003

The one decision as Duomed, Inc. →