FDA applicant

Liaoning-Usa Corp.

Pasadena, CA6 decisions1989–19910 recalls

FDA records 6 decisions for Liaoning-Usa Corp. (Pasadena, CA) from 1989 to 1991: 6 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) and FLK (Thermometer, Clinical Mercury). 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 Liaoning-Usa Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Liaoning-Usa Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Liaoning-Usa Corp.

Which product codes does it file in?

What has FDA decided for it lately?