Dynawave, Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
What Dynawave, Corp. makes
Dynawave Corp. manufactures therapeutic ultrasound stimulators, including the DYNASOUND 601, DYNASOUND 801, and DYNASOUND Model 401. These devices are designed for medical applications involving ultrasound-based stimulation or therapy.
The company’s products fall under FDA Class II devices and are listed via 510(k) clearance. Dynawave Corp. is based in the United States.
Catalogue
Dynasound 601 Ref K791976
510(k) 510(k)Dynasound 801 Ref K811159
510(k) 510(k)- 510(k) 510(k)
Frequently asked questions
How many devices does Dynawave, Corp. have in the registry?
The registry currently lists 3 devices for Dynawave, Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dynawave, Corp.'s devices?
Among its 3 most recently registered devices, Dynawave, Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Dynawave, Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Dynawave, Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dynawave, Corp. in the registry?
The most recently registered devices listed for Dynawave, Corp. include DYNASOUND 601, DYNASOUND 801 and DYNASOUND MODEL 401 THERAPEUTIC ULTRASOUND STIMULATOR.