510(k) Report

FDA applicant

National Therapy Products, Inc.

Woodbridge, Ontario, CA2 decisions2001–20020 recalls

FDA records 2 decisions for National Therapy Products, Inc. (Woodbridge, Ontario, CA) from 2001 to 2002: 2 510(k) clearances. Most are in product codes ITX (Transducer, Ultrasonic, Diagnostic) and MUI (Media, Coupling, Ultrasound). 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, radiology panel, where it files most

How often FDA has decided National Therapy Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for National Therapy Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — National Therapy Products, 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?

  • ITXTransducer, Ultrasonic, Diagnostic1decision
  • MUIMedia, Coupling, Ultrasound1decision

What has FDA decided for it lately?

  • K013212Wavelenght Ultrasound LotionNational Therapy Products, Inc. · 2002
  • K012522Wavelength Multi-Purpose Ultrasound GelNational Therapy Products, Inc. · 2001

All 2 as National Therapy Products, Inc. →