FDA applicant
Felda Rubber Corp.
FDA records 2 decisions for Felda Rubber Corp. (50200 Kuala Lumpur, MY) from 1989 to 1999: 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 Felda Rubber Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Felda Rubber Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Felda Rubber Corp.’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