FDA applicant

Camdent Laboratories

Mchenry, IL1 decision1982–19820 recalls

FDA records 1 decision for Camdent Laboratories (Mchenry, IL) in 1982: 1 510(k) clearance. All are in product code EBO (Denture Repair Kit). 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 Camdent Laboratories’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Camdent Laboratories since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Camdent Laboratories

Which product codes does it file in?

What has FDA decided for it lately?