FDA applicant

Prodent Intl., Inc.

Chicago, IL2 decisions1987–19900 recalls

FDA records 2 decisions for Prodent Intl., Inc. (Chicago, IL) from 1987 to 1990: 2 510(k) clearances. Most are in product codes ELC (Scaler, Ultrasonic) and EFH (Paper, Articulation). 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 Prodent Intl., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Prodent Intl., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Prodent Intl., Inc.

Which product codes does it file in?

What has FDA decided for it lately?