510(k) Report

FDA applicant

Steven Lamberg, D.D.S

Washington, DC1 decision2006–20060 recalls

FDA records 1 decision for Steven Lamberg, D.D.S (Washington, DC) in 2006: 1 510(k) clearance. All are in product code LRK (Device, Anti-Snoring). Its devices cite 3 predicates, 0 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 Steven Lamberg, D.D.S’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Steven Lamberg, D.D.S since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Steven Lamberg, D.D.S 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-Snoring1decision

Whose devices does it build on?

Its devices cite 3 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 2 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.

  • K062333LaimadSteven Lamberg, D.D.S · 20062cite it

What has FDA decided for it lately?

  • K062333LaimadSteven Lamberg, D.D.S · 2006

The one decision as Steven Lamberg, D.D.S →

Other applicant names beginning “Steven”

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

Steven H. Warnock, M.D. 1Steven Frank Mercereau 1Steven B. Lamberg, Dds 1Steven K. Juhn 1Steven K. Sue 1Steven Chen 1