510(k) Report

FDA applicant

The Dezac Group

Washington, DC3 decisions2002–20020 recalls

FDA records 3 decisions for The Dezac Group (Washington, DC) in 2002: 3 510(k) clearances. Most are in product codes NGX (Stimulator, Muscle, Powered, For Muscle…) and GYB (Media, Electroconductive). 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, physical medicine panel, where it files most

How often FDA has decided The Dezac Group’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Dezac Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — The Dezac Group 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?

  • NGXStimulator, Muscle, Powered, For Muscle Conditioning2decisions
  • GYBMedia, Electroconductive1decision

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.

  • K022006Conductive GelThe Dezac Group · 20022cite it

What has FDA decided for it lately?

  • K022006Conductive GelThe Dezac Group · 2002
  • K020427AB BeltThe Dezac Group · 2002
  • K020429AB Belt ProThe Dezac Group · 2002

All 3 as The Dezac Group →