510(k) Report

FDA applicant

Usa Laser Therapeutics, Inc.

Houston, TX1 decision2007–20070 recalls

FDA records 1 decision for Usa Laser Therapeutics, Inc. (Houston, TX) in 2007: 1 510(k) clearance. 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 Usa Laser Therapeutics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2007

2007: 1
2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Usa Laser Therapeutics, 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 Relief1decision

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.

  • K052836Bodihealth SystemUsa Laser Therapeutics, Inc. · 20072cite it

What has FDA decided for it lately?

  • K052836Bodihealth SystemUsa Laser Therapeutics, Inc. · 2007

The one decision as Usa Laser Therapeutics, Inc. →