510(k) Report

FDA applicant

Snorefree, Inc.

East Islip, NY1 decision1996–19960 recalls

FDA records 1 decision for Snorefree, Inc. (East Islip, NY) in 1996: 1 510(k) clearance. All are in product code LQZ (Device, Jaw Repositioning). 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 Snorefree, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Snorefree, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Snorefree, Inc. 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?

  • LQZDevice, Jaw Repositioning1decision

Who builds on its devices?

Later devices cite its devices 3 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.

  • K960673OSAPSnorefree, Inc. · 19963cite it

What has FDA decided for it lately?

The one decision as Snorefree, Inc. →