Vertos Medical, Inc.
Country not established
- Devices
- 1
What Vertos Medical, Inc. makes
Vertos Medical, Inc. manufactures the Vertos mild Device Kit (MDK-0002), a surgical implant system designed for cochlear implantation procedures in adults with mild-to-severe sensorineural hearing loss.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices and is listed in the FDA’s 510(k) database. Vertos Medical, Inc. is based in the United States.
Catalogue
Vertos mild Device Kit (MDK-0002) Ref K233800
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vertos Medical, Inc. have in the registry?
The registry currently lists 1 device for Vertos Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vertos Medical, Inc.'s devices?
Among its 1 most recently registered device, Vertos Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Vertos Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Vertos Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vertos Medical, Inc. in the registry?
The most recently registered devices listed for Vertos Medical, Inc. include Vertos mild Device Kit (MDK-0002).