FDA applicant

Besglove Healthcare Sdn. Bhd.

Selangor, MY1 decision1997–19970 recalls

FDA records 1 decision for Besglove Healthcare Sdn. Bhd. (Selangor, MY) in 1997: 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 Besglove Healthcare Sdn. Bhd.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Besglove Healthcare 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 Medicare Sdn. Bhd. 22

Besglove Healthcare Sdn. Bhd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Besglove”