FDA applicant

Aladan Corp.

Dothan, AL18 decisions1989–19960 recalls

FDA records 18 decisions for Aladan Corp. (Dothan, AL) from 1989 to 1996: 18 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) and HIS (Condom). 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, general hospital panel, where it files most

How often FDA has decided Aladan Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Aladan Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Aladan Corp.

Which product codes does it file in?

What has FDA decided for it lately?