FDA applicant

Dentronix, Inc.

Mchenry, IL9 decisions1977–19910 recalls

FDA records 9 decisions for Dentronix, Inc. (Mchenry, IL) from 1977 to 1991: 9 510(k) clearances. Most are in product codes FZT (Cutter, Surgical) and HTZ (Instrument, Cutting, Orthopedic). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Dentronix, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dentronix, 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?