510(k) Report

FDA applicant

Mavidon Medical Products

Lake Worth, FL1 decision2001–20010 recalls

FDA records 1 decision for Mavidon Medical Products (Lake Worth, FL) in 2001: 1 510(k) clearance. All are in product code GYB (Media, Electroconductive). 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 Mavidon Medical Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mavidon Medical Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Mavidon Medical Products 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?

  • GYBMedia, Electroconductive1decision

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.

  • K003924Mavidon Medical Electrode JellyMavidon Medical Products · 20011cites it

What has FDA decided for it lately?

  • K003924Mavidon Medical Electrode JellyMavidon Medical Products · 2001

The one decision as Mavidon Medical Products →