FDA applicant
Young and Moore Enterprises, Inc.
FDA records 1 decision for Young and Moore Enterprises, Inc. (Phoenix, AZ) in 1987: 1 510(k) clearance. All are in product code LPN (Accessories, Soft Lens Products). 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 Young and Moore Enterprises, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Young and Moore Enterprises, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Young and Moore Enterprises, 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 “Young”
FDA records each applicant name separately; these may or may not be the same firm.