510(k) Report

FDA applicant

D.D.S., Inc.

Half Moon Bay, CA1 decision1995–19950 recalls

FDA records 1 decision for D.D.S., Inc. (Half Moon Bay, CA) in 1995: 1 510(k) clearance. 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 D.D.S., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for D.D.S., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like D.D.S., 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

Which product codes does it file in?

  • LRKDevice, Anti-Snoring1decision

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.

  • K954128SnoremasterD.D.S., Inc. · 19953cite it

What has FDA decided for it lately?

  • K954128SnoremasterD.D.S., Inc. · 1995

The one decision as D.D.S., Inc. →