FDA applicant
Naturub Sdn. Bhd.
FDA records 3 decisions for Naturub Sdn. Bhd. (Malaysia, MY) from 1989 to 1990: 3 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) and EIE (Dam, Rubber). 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 Naturub Sdn. Bhd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Naturub Sdn. Bhd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Naturub 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