FDA applicant

Ct Intl.

San Luis Obispo, CA3 decisions1989–19990 recalls

FDA records 3 decisions for Ct Intl. (San Luis Obispo, CA) from 1989 to 1999: 3 510(k) clearances. Most are in product codes KGO (Surgeon'S Gloves) and LZA (Polymer Patient Examination Glove). 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 and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Ct Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Ct Intl.

Which product codes does it file in?

What has FDA decided for it lately?