FDA applicant

J.L. Blosser, Inc.

Liberty, MO2 decisions1993–20040 recalls

FDA records 2 decisions for J.L. Blosser, Inc. (Liberty, MO) from 1993 to 2004: 2 510(k) clearances. Most are in product codes EMA (Cement, Dental) and EBZ (Activator, Ultraviolet, For Polymerization). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 J.L. Blosser, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for J.L. Blosser, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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J.L. Blosser, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?