FDA applicant

Cadema Medical Products, Inc.

Middletown, NY6 decisions1985–19900 recalls

FDA records 6 decisions for Cadema Medical Products, Inc. (Middletown, NY) from 1985 to 1990: 6 510(k) clearances. Most are in product codes CAF (Nebulizer (Direct Patient Interface)) and CAH (Filter, Bacterial, Breathing-Circuit). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Cadema Medical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Cadema Medical Products, Inc.

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?