Claret Medical, Inc.
Country not established
- Devices
- 1
What Claret Medical, Inc. makes
Claret Medical, Inc. makes the Sentinel Cerebral Protection System, a device designed to capture and remove debris during transcatheter aortic valve replacement procedures to reduce the risk of stroke.
The Sentinel Cerebral Protection System is classified as a Class II medical device and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Sentinel Cerebral Protection System Ref DEN160043
Regimes: De Novo Registry: De Novo
Frequently asked questions
How many devices does Claret Medical, Inc. have in the registry?
The registry currently lists 1 device for Claret Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Claret Medical, Inc.'s devices?
Among its 1 most recently registered device, Claret Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Claret Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Claret Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Claret Medical, Inc. in the registry?
The most recently registered devices listed for Claret Medical, Inc. include Sentinel Cerebral Protection System.