FDA applicant

Ndm Corp.

Mchenry, IL11 decisions1976–19930 recalls

FDA records 11 decisions for Ndm Corp. (Mchenry, IL) from 1976 to 1993: 11 510(k) clearances. Most are in product codes DRX (Electrode, Electrocardiograph) and GEI (Electrosurgical, Cutting & Coagulation &…). 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 and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Ndm Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Ndm Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?