FDA applicant
Bright Rubber Industries Private, Ltd.
FDA records 1 decision for Bright Rubber Industries Private, Ltd. (India, IN) in 1990: 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
How often FDA has decided Bright Rubber Industries Private, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Bright Rubber Industries Private, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Bright Rubber Industries Private, Ltd.’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) ReportOther applicant names beginning “Bright”
FDA records each applicant name separately; these may or may not be the same firm.