FDA applicant

Liwe Trading

Selangor Darul Ehsan, MY4 decisions1991–20070 recalls

FDA records 4 decisions for Liwe Trading (Selangor Darul Ehsan, MY) from 1991 to 2007: 4 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) 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 hospital panel, where it files most

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

FDA decisions per year

2in 2007

2007high 2 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Liwe Trading

Which product codes does it file in?

What has FDA decided for it lately?