Keravision, Inc.
Country not established
- Devices
- 1
What Keravision, Inc. makes
Keravision, Inc. makes the Keravision Vacuum Ring System.
The device is classified as Class I and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Keravision Vacuum Ring System Ref K984540
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Keravision, Inc. have in the registry?
The registry currently lists 1 device for Keravision, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Keravision, Inc.'s devices?
Among its 1 most recently registered device, Keravision, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Keravision, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Keravision, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Keravision, Inc. in the registry?
The most recently registered devices listed for Keravision, Inc. include KERAVISION VACUUM RING SYSTEM.