510(k) Report

FDA applicant

Medical Device Marketing Network, Inc.

Cleveland, OH1 decision1990–19900 recalls

FDA records 1 decision for Medical Device Marketing Network, Inc. (Cleveland, OH) in 1990: 1 510(k) clearance. All are in product code IZH (System, X-Ray, Mammographic). 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, radiology panel, where it files most

How often FDA has decided Medical Device Marketing Network, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Device Marketing Network, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medical Device Marketing Network, Inc. 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?

  • IZHSystem, X-Ray, Mammographic1decision

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.

  • K901558Giotto Mammography HFMedical Device Marketing Network, Inc. · 19901cites it

What has FDA decided for it lately?

  • K901558Giotto Mammography HFMedical Device Marketing Network, Inc. · 1990

The one decision as Medical Device Marketing Network, Inc. →