Avra Corp.
Country not established
- Devices
- 1
What Avra Corp. makes
Avra Corp. manufactures the Galvanator Model 770, an electrotherapy device designed for transcutaneous electrical nerve stimulation (TENS) and muscle stimulation therapies.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The device is listed in the FDA’s 510(k) registry. Avra Corp. is based in the United States.
Catalogue
Galvanator, Model 770 Ref K781080
510(k) 510(k)
Frequently asked questions
How many devices does Avra Corp. have in the registry?
The registry currently lists 1 device for Avra Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Avra Corp.'s devices?
Among its 1 most recently registered device, Avra Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Avra Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Avra Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Avra Corp. in the registry?
The most recently registered devices listed for Avra Corp. include GALVANATOR, MODEL 770.