510(k) Report

FDA applicant

Maven Labs, Inc.

Washington, DC2 decisions1991–19970 recalls

FDA records 2 decisions for Maven Labs, Inc. (Washington, DC) from 1991 to 1997: 2 510(k) clearances. All are in product code GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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, neurology panel, where it files most

How often FDA has decided Maven Labs, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Maven Labs, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Maven Labs, 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?

  • GZJStimulator, Nerve, Transcutaneous, For Pain Relief2decisions

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K961050Reliefband Tens Unit (Modification)Maven Labs, Inc. · 19971cites it

What has FDA decided for it lately?

  • K961050Reliefband Tens Unit (Modification)Maven Labs, Inc. · 1997
  • K901704Relief Band (T.E.N.S. Device)Maven Labs, Inc. · 1991

All 2 as Maven Labs, Inc. →