FDA applicant

Denplus, Inc.

Montreal, Quebec, CA2 decisions1999–20010 recalls

FDA records 2 decisions for Denplus, Inc. (Montreal, Quebec, CA) from 1999 to 2001: 2 510(k) clearances. All are in product code 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 Denplus, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Denplus, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Denplus, Inc.

Which product codes does it file in?

What has FDA decided for it lately?