FDA applicant
Always More Marketing, Inc.
FDA records 4 decisions for Always More Marketing, Inc. (Las Vegas, NV) from 2011 to 2019: 4 510(k) clearances. All are in product code LRK (Device, Anti-Snoring). Its devices cite 18 predicates, 3 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Always More Marketing”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Always More Marketing, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2019
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2011.
Planning a device like Always More Marketing, 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