Dynatronics Laser Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 5
What Dynatronics Laser Corp. makes
Dynatronics Laser Corp. manufactures electrical point stimulators, body composition analyzers, EMG/biofeedback analyzers, and ultrasound devices.
The company's products are listed in the FDA 510(k) registry and are classified as Class II medical devices. Dynatronics Laser Corp. is based in the US.
Catalogue
Dynatron 1120 Eps (Electrical Point Stimulator) Ref K864370
510(k) 510(k)Dynatron Ii Ref K880464
510(k) 510(k)Dynatron 330 Body Composition Analyzer Ref K900321
510(k) 510(k)Dynatron 350 Emg/Biofeedback Analyzer Ref K900639
510(k) 510(k)Dynatron 300 Ulrasound Ref K920939
510(k) 510(k)
Frequently asked questions
How many devices does Dynatronics Laser Corp. have in the registry?
The registry currently lists 5 devices for Dynatronics Laser Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dynatronics Laser Corp.'s devices?
Among its 5 most recently registered devices, Dynatronics Laser Corp. has devices listed in FDA 510(k) (5 devices).
What risk classes do Dynatronics Laser Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Dynatronics Laser Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dynatronics Laser Corp. in the registry?
The most recently registered devices listed for Dynatronics Laser Corp. include DYNATRON 1120 EPS (ELECTRICAL POINT STIMULATOR), DYNATRON II, DYNATRON 330 BODY COMPOSITION ANALYZER and DYNATRON 350 EMG/BIOFEEDBACK ANALYZER.