FDA applicant

Dynatronics Laser Corp.

Salt Lake City, UT5 decisions1987–19930 recalls

FDA records 5 decisions for Dynatronics Laser Corp. (Salt Lake City, UT) from 1987 to 1993: 5 510(k) clearances. Most are in product codes IMG (Stimulator, Ultrasound And Muscle, For Use In…) and LBB (Dynamometer, Ac-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 Laser Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dynatronics Laser Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dynatronics Laser Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Dynatronics Laser Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Dynatronics”

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

Dynatronics Corp. 25 Dynatronics Research Corp. 2

Dynatronics Laser Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Dynatronics”