FDA applicant

Diemolding Corp.

Canastota, NY12 decisions1976–19960 recalls

FDA records 12 decisions for Diemolding Corp. (Canastota, NY) from 1976 to 1996: 12 510(k) clearances. Most are in product codes BWF (Spirometer, Therapeutic (Incentive)) and CCQ (Nebulizer, Medicinal, Non-Ventilatory (Atomizer)). 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 Diemolding Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Diemolding Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Diemolding 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?