FDA applicant
Gloveco, Inc.
FDA records 1 decision for Gloveco, Inc. (Chino, CA) in 2005: 1 510(k) clearance. All are in product code LYZ (Vinyl Patient Examination Glove). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 Gloveco, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Gloveco, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Gloveco, 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) Report