FDA applicant
Mulpha Intl. Trading Corp. Bhd.
FDA records 6 decisions for Mulpha Intl. Trading Corp. Bhd. (Selangor, Malaysia, MY) in 1989: 6 510(k) clearances. 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
How often FDA has decided Mulpha Intl. Trading Corp. Bhd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Mulpha Intl. Trading Corp. Bhd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Mulpha Intl. Trading Corp. 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