FDA applicant

Demetron Research Corp.

Mchenry, IL4 decisions1978–19960 recalls

FDA records 4 decisions for Demetron Research Corp. (Mchenry, IL) from 1978 to 1996: 4 510(k) clearances. Most are in product codes EBZ (Activator, Ultraviolet, For Polymerization) and EBD (Coating, Filling Material, 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 Demetron Research Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Demetron Research Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Demetron Research Corp.’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

Demetron Research Corp.

Which product codes does it file in?

What has FDA decided for it lately?