510(k) Report

FDA applicant

Snore - Ezzer

Waukesha, WI2 decisions1998–19990 recalls

FDA records 2 decisions for Snore - Ezzer (Waukesha, WI) from 1998 to 1999: 2 510(k) clearances. All are in product code LRK (Device, Anti-Snoring). 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 Snore - Ezzer’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Snore - Ezzer since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Snore - Ezzer by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • LRKDevice, Anti-Snoring2decisions

Who builds on its devices?

Later devices cite its devices 4 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K991948DR. B'S Mouthpiece, Model 32129-10002Snore - Ezzer · 19994cite it

What has FDA decided for it lately?

  • K991948DR. B'S Mouthpiece, Model 32129-10002Snore - Ezzer · 1999
  • K974531Snore-EzzerSnore - Ezzer · 1998

All 2 as Snore - Ezzer →

Other applicant names beginning “Snore”

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

The Snore Reliever Company, LLC 2The Snore Peace Group 1