FDA applicant

North American Medical Products, Inc.

Loudonville, NY6 decisions1984–20010 recalls

FDA records 6 decisions for North American Medical Products, Inc. (Loudonville, NY) from 1984 to 2001: 6 510(k) clearances. Most are in product codes FMI (Needle, Hypodermic, Single Lumen) and EOQ (Bronchoscope (Flexible Or Rigid)). 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, ear, nose and throat panel, where it files most

How often FDA has decided North American Medical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for North American Medical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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North American Medical Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?