FDA applicant

Midian Intl.

Lauderhill, FL1 decision1998–19980 recalls

FDA records 1 decision for Midian Intl. (Lauderhill, FL) in 1998: 1 510(k) clearance. All are in product code EFS (Unit, Oral Irrigation). 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 Midian Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Midian Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Midian Intl.

Which product codes does it file in?

What has FDA decided for it lately?