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Dynatronics Corp.

Also registered as Dynatronics Corporation

United StatesFDA applicant, unverified

Dynatronics Corp. is a medical device manufacturer, with 130 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 13 Nov 2026.

Devices
130

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 105
  • FDA 510(k) 25

A device listed in two registries counts in both.

Device classes
  • FDA Class II 128
  • FDA Class I 2

What Dynatronics Corp. makes

Dynatronics Corp. manufactures transcutaneous electrical stimulation electrodes and leads, multi-modality physical therapy systems, ultrasound system applicators and systems, intermittent powered traction systems, light-energy skin surface treatment system applicators, and skin topical coupling gels and lotions for professional-use physical therapy settings.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue130

Newest first, rows 1-50 of 130

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Rows 1-50 of 130

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Frequently asked questions

How many devices does Dynatronics Corp. have in the registry?

The registry currently lists 130 devices for Dynatronics Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dynatronics Corp.'s devices?

Among its 50 most recently registered devices, Dynatronics Corp. has devices listed in FDA GUDID (50 devices).

What risk classes do Dynatronics Corp.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for Dynatronics Corp.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Dynatronics Corp. in the registry?

The most recently registered devices listed for Dynatronics Corp. include Digital Portable EMS DGEMS, DynaFlex Brown 1.5"x3.5" DF2.75R, Superior Cloth Electrodes 2"x4" DSC2X4-CS and Dynatron Ion Butterfly Ion-B.

Generated automatically from registry data and not verified by a human reviewer.