FDA applicant

Besglove Medicare Sdn. Bhd.

Selangor Darul Ehsan, MY22 decisions1997–20000 recalls

FDA records 22 decisions for Besglove Medicare Sdn. Bhd. (Selangor Darul Ehsan, MY) from 1997 to 2000: 22 510(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 Besglove Medicare Sdn. Bhd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Besglove Medicare Sdn. Bhd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Besglove Medicare Sdn. Bhd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Besglove”

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

Besglove Healthcare Sdn. Bhd. 1

Besglove Medicare Sdn. 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 “Besglove”