510(k) Report

FDA applicant

Always More Marketing, Inc.

Las Vegas, NV4 decisions2011–20190 recalls

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, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

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

2011: 12012: 22019: 1
2011high 2 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Always More Marketing, Inc. by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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.

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