510(k) Report

FDA applicant

Dynatronics Research Corp.

Salt Lake City, UT2 decisions1993–19950 recalls

FDA records 2 decisions for Dynatronics Research Corp. (Salt Lake City, UT) from 1993 to 1995: 2 510(k) clearances. Most are in product codes LIH (Interferential Current Therapy) and IPF (Stimulator, Muscle, Powered). 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 Dynatronics Research Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dynatronics Research Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dynatronics Research Corp. 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?

  • LIHInterferential Current Therapy1decision
  • IPFStimulator, Muscle, Powered1decision

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.

  • K941461Dynatron 850Dynatronics Research Corp. · 19951cites it

What has FDA decided for it lately?

  • K941461Dynatron 850Dynatronics Research Corp. · 1995
  • K933249Dynatron 100 PlusDynatronics Research Corp. · 1993

All 2 as Dynatronics Research Corp. →

Other applicant names beginning “Dynatronics”

FDA records each applicant name separately; these may or may not be the same firm.

Dynatronics Corp. 25Dynatronics Laser Corp. 5