FDA applicant
Ever Surplus (Usa), Inc.
FDA records 2 decisions for Ever Surplus (Usa), Inc. (New York City, NY) 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 Ever Surplus (Usa), Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Ever Surplus (Usa), Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Ever Surplus (Usa), Inc.’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 “Ever”
FDA records each applicant name separately; these may or may not be the same firm.