FDA applicant

Laurentian Laboratories

Mchenry, IL2 decisions1984–19840 recalls

FDA records 2 decisions for Laurentian Laboratories (Mchenry, IL) in 1984: 2 510(k) clearances. 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 Laurentian Laboratories’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Laurentian Laboratories since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Laurentian Laboratories

Which product codes does it file in?

What has FDA decided for it lately?