FDA applicant

Grand Design Sdn. Bhd.

Malaysia, MY1 decision1989–19890 recalls

FDA records 1 decision for Grand Design Sdn. Bhd. (Malaysia, MY) in 1989: 1 510(k) clearance. 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 Grand Design Sdn. Bhd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Grand Design Sdn. Bhd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Grand Design Sdn. 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 “Grand”

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

Grand Work Plastic Products Co., Ltd. 19 Grand Medical Products 8 Grand Monde Trading Co., Inc. 2 Grand Universe Trading Co., Ltd. 1 Grand Traverse Technologies 1 Grand Seating King Corp. 1 Grand Imperial, Inc. 1

Grand Design Sdn. Bhd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Grand”