FDA applicant

Health Products, Inc.

Cedar Grove, NJ13 decisions1986–19920 recalls

FDA records 13 decisions for Health Products, Inc. (Cedar Grove, NJ) from 1986 to 1992: 13 510(k) clearances. Most are in product codes BWF (Spirometer, Therapeutic (Incentive)) and BZH (Meter, Peak Flow, Spirometry). 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 Health Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Health Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Health 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?