FDA applicant

M.R.G. Industries Berhad

Kamunting, MY1 decision1999–19990 recalls

FDA records 1 decision for M.R.G. Industries Berhad (Kamunting, MY) in 1999: 1 510(k) clearance. All are in product code 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 M.R.G. Industries Berhad’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for M.R.G. Industries Berhad since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — M.R.G. Industries Berhad by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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M.R.G. Industries Berhad

Which product codes does it file in?

What has FDA decided for it lately?