FDA applicant
Anro Corp. Sdn Bhd
FDA records 2 decisions for Anro Corp. Sdn Bhd (Richardson, TX) in 1989: 2 510(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 Anro Corp. Sdn Bhd’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Anro Corp. Sdn Bhd since 2007.
Recalls per year
No recall linked to its devices since 2007.
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