FDA applicant

E.C. Moore Co.

Walker, MI1 decision1979–19790 recalls

FDA records 1 decision for E.C. Moore Co. (Walker, MI) in 1979: 1 510(k) clearance. All are in product code EHJ (Disk, Abrasive). 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 E.C. Moore Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for E.C. Moore Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like E.C. Moore Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

E.C. Moore Co.

Which product codes does it file in?

What has FDA decided for it lately?