FDA applicant

Hoyt Laboratories

Mchenry, IL11 decisions1977–19820 recalls

FDA records 11 decisions for Hoyt Laboratories (Mchenry, IL) from 1977 to 1982: 11 510(k) clearances. Most are in product codes EFW (Toothbrush, Manual) and EBF (Material, Tooth Shade, Resin). 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, dental panel, where it files most

How often FDA has decided Hoyt Laboratories’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hoyt Laboratories since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Hoyt Laboratories

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?