FDA applicant

The Snore Reliever Company, LLC

Laguna Niguel, CA2 decisions2010–20210 recalls

FDA records 2 decisions for The Snore Reliever Company, LLC (Laguna Niguel, CA) from 2010 to 2021: 2 510(k) clearances. All are in product code LRK (Device, Anti-Snoring). Its devices cite 2 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

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 The Snore Reliever Company, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — The Snore Reliever Company, LLC by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like The Snore Reliever Company, LLC’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

Other applicant names beginning “The”

FDA records each applicant name separately; these may or may not be the same firm.

Snore - Ezzer 2 The Snore Peace Group 1

The Snore Reliever Company, LLC

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “The”