Dynatronics Research Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Dynatronics Research Corp. makes
Dynatronics Research Corp. manufactures electrotherapy devices, including the Dynatron 100 Plus and Dynatron 850, which are designed for transcutaneous electrical nerve stimulation (TENS) and muscle stimulation therapies. These devices are intended for pain management and physical rehabilitation applications, delivering controlled electrical impulses to targeted muscle groups or nerve pathways.
The company’s portfolio is regulated under Class II medical devices in the United States, with individual products authorised through the FDA’s 510(k) clearance process. These devices are listed in the FDA’s 510(k) registry, ensuring compliance with U.S. medical device regulations. The manufacturer operates from the United States.
Catalogue
Dynatron 100 Plus Ref K933249
510(k) 510(k)Dynatron 850 Ref K941461
510(k) 510(k)
Frequently asked questions
How many devices does Dynatronics Research Corp. have in the registry?
The registry currently lists 2 devices for Dynatronics Research Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dynatronics Research Corp.'s devices?
Among its 2 most recently registered devices, Dynatronics Research Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Dynatronics Research Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Dynatronics Research Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dynatronics Research Corp. in the registry?
The most recently registered devices listed for Dynatronics Research Corp. include DYNATRON 100 PLUS and DYNATRON 850.