510(k) Report

FDA applicant

Myerson Tooth Corp.

Mchenry, IL2 decisions1980–19800 recalls

FDA records 2 decisions for Myerson Tooth Corp. (Mchenry, IL) in 1980: 2 510(k) clearances. Most are in product codes ELL (Teeth, Porcelain) and EBG (Crown And Bridge, Temporary, 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 Myerson Tooth Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Myerson Tooth Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Myerson”

FDA records each applicant name separately; these may or may not be the same firm.