FDA applicant
Us Clover Co.
FDA records 1 decision for Us Clover Co. (City Of Industry, CA) in 2005: 1 510(k) clearance. All are in product code DQK (Computer, Diagnostic, Programmable). 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 Us Clover Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Us Clover Co. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Us Clover Co.’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