FDA applicant

Wallace A. Erickson & Co.

Chicago, IL32 decisions1978–19990 recalls

FDA records 32 decisions for Wallace A. Erickson & Co. (Chicago, IL) from 1978 to 1999: 32 510(k) clearances. Most are in product codes EBF (Material, Tooth Shade, Resin) and DYH (Adhesive, Bracket And Tooth Conditioner, 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 Wallace A. Erickson & Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Wallace A. Erickson & Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Wallace A. Erickson & Co.

Which product codes does it file in?

What has FDA decided for it lately?