Deravox, Inc.
Country not established
- Devices
- 1
What Deravox, Inc. makes
Deravox, Inc. makes the DANAVOS CUSTOM EAR device.
The DANAVOS CUSTOM EAR is a Class I medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Danavos Custom Ear Ref K821991
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Deravox, Inc. have in the registry?
The registry currently lists 1 device for Deravox, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Deravox, Inc.'s devices?
Among its 1 most recently registered device, Deravox, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Deravox, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Deravox, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Deravox, Inc. in the registry?
The most recently registered devices listed for Deravox, Inc. include DANAVOS CUSTOM EAR.