510(k) Report

FDA applicant

Denpac Corp.

Mchenry, IL4 decisions1980–19870 recalls

FDA records 4 decisions for Denpac Corp. (Mchenry, IL) from 1980 to 1987: 4 510(k) clearances. Most are in product codes EMA (Cement, Dental) and EJS (Alloy, Other Noble Metal). 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 Denpac Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Denpac Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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