510(k) Report

FDA applicant

Apl International Incorporated Limited

Dong Nau, VN2 decisions2004–20040 recalls

FDA records 2 decisions for Apl International Incorporated Limited (Dong Nau, VN) in 2004: 2 510(k) clearances. All are in product code LYY (Latex 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 Apl International Incorporated Limited’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Apl International Incorporated Limited since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • LYYLatex Patient Examination Glove2decisions

What has FDA decided for it lately?

  • K033533Powder Free Latex Examination GlovesApl International Incorporated Limited · 2004
  • K033531Powdered Latex Examination GlovesApl International Incorporated Limited · 2004

All 2 as Apl International Incorporated Limited →