FDA applicant

Leach and Dillon Co., Inc.

Mansfield, MA31 decisions1989–19910 recalls

FDA records 31 decisions for Leach and Dillon Co., Inc. (Mansfield, MA) from 1989 to 1991: 31 510(k) clearances. Most are in product codes EJT (Alloy, Gold-Based Noble Metal) and EJH (Alloy, Metal, Base). 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 Leach and Dillon Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Leach and Dillon Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Leach and Dillon Co., Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?