FDA applicant

E&D Dental Manufacturing Co.

Hillside, NJ6 decisions1986–19880 recalls

FDA records 6 decisions for E&D Dental Manufacturing Co. (Hillside, NJ) from 1986 to 1988: 6 510(k) clearances. Most are in product codes EMB (Zinc Oxide Eugenol) and EBI (Resin, Denture, Relining, Repairing, Rebasing). 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&D Dental Manufacturing Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for E&D Dental Manufacturing Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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E&D Dental Manufacturing Co.

Which product codes does it file in?

What has FDA decided for it lately?