FDA applicant
World Wide Outdoor Marketing
FDA records 1 decision for World Wide Outdoor Marketing (Minden, LA) in 1984: 1 510(k) clearance. All are in product code DZN (Instruments, Dental Hand). 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 World Wide Outdoor Marketing’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for World Wide Outdoor Marketing since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like World Wide Outdoor Marketing’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