Earbear Co.
Country not established
- Devices
- 1
What Earbear Co. makes
Earbear Co. manufactures the EARBEAR OTOSCOPE, a medical device used for examining the ear canal and eardrum.
The company is based in the US and its products are listed in the FDA 510(k) registry as Class I devices.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Earbear Otoscope Ref K915537
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Earbear Co. have in the registry?
The registry currently lists 1 device for Earbear Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Earbear Co.'s devices?
Among its 1 most recently registered device, Earbear Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Earbear Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Earbear Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Earbear Co. in the registry?
The most recently registered devices listed for Earbear Co. include EARBEAR OTOSCOPE.