FDA applicant

Latexx Partners Bhd.

Kamunting, Perak, MY7 decisions1998–20010 recalls

FDA records 7 decisions for Latexx Partners Bhd. (Kamunting, Perak, MY) from 1998 to 2001: 7 510(k) clearances. Most are in product codes LZA (Polymer Patient Examination Glove) and 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 Latexx Partners Bhd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Latexx Partners Bhd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Latexx”

FDA records each applicant name separately; these may or may not be the same firm.

Latexx Manufacturing Sdn.Bhd. 10 Latexx Partners, Inc. 1

Latexx Partners Bhd.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Latexx”