FDA applicant

Dennison Manufacturing Co.

Mchenry, IL1 decision1976–19760 recalls

FDA records 1 decision for Dennison Manufacturing Co. (Mchenry, IL) in 1976: 1 510(k) clearance. All are in product code JLG (Conversion To Ferric Hydroxymates…). 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, clinical chemistry panel, where it files most

How often FDA has decided Dennison Manufacturing Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dennison Manufacturing Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dennison Manufacturing Co.

Which product codes does it file in?

What has FDA decided for it lately?