510(k) Report

FDA applicant

Albert J. Anthony, Dmd

Mchenry, IL1 decision1981–19810 recalls

FDA records 1 decision for Albert J. Anthony, Dmd (Mchenry, IL) in 1981: 1 510(k) clearance. All are in product code DZC (Wire, Orthodontic). 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 Albert J. Anthony, Dmd’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Albert J. Anthony, Dmd since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • DZCWire, Orthodontic1decision

What has FDA decided for it lately?

  • K812454Pac-AidAlbert J. Anthony, Dmd · 1981

The one decision as Albert J. Anthony, Dmd →

Other applicant names beginning “Albert”

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

Albert Browne, Ltd. 19Albert K. Chin 1Albert Davydov Dds PC Professional 1