Eyevi & Co.
Country not established
- Devices
- 1
What Eyevi & Co. makes
Eyevi & Co. manufactures EYEWI ANKORS, which are Class I medical devices.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
Eyewi Ankors Ref K800726
510(k) 510(k)
Frequently asked questions
How many devices does Eyevi & Co. have in the registry?
The registry currently lists 1 device for Eyevi & Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eyevi & Co.'s devices?
Among its 1 most recently registered device, Eyevi & Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Eyevi & Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Eyevi & Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Eyevi & Co. in the registry?
The most recently registered devices listed for Eyevi & Co. include EYEWI ANKORS.