510(k) Report

FDA applicant

Pro Message Co.

Denver, CO1 decision1990–19900 recalls

FDA records 1 decision for Pro Message Co. (Denver, CO) in 1990: 1 510(k) clearance. All are in product code LYG (Massager, Therapeutic, Manual). 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 Pro Message Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pro Message Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Pro Message Co. 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?

  • LYGMassager, Therapeutic, Manual1decision

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.

  • K903820Thera-CanePro Message Co. · 19901cites it

What has FDA decided for it lately?

  • K903820Thera-CanePro Message Co. · 1990

The one decision as Pro Message Co. →