510(k) Report

FDA applicant

L.D. Caulk Co.

Mchenry, IL21 decisions1976–19810 recalls

FDA records 21 decisions for L.D. Caulk Co. (Mchenry, IL) from 1976 to 1981: 20 510(k) clearances and 1 original PMA approval. Most are in product codes EBF (Material, Tooth Shade, Resin) and DYH (Adhesive, Bracket And Tooth Conditioner, 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 L.D. Caulk Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for L.D. Caulk Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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