Colibri Technologies, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Colibri Technologies, Inc. makes
Colibri Technologies, Inc. manufactures the Foresight Intracardiac Echocardiography (ICE) System, a device used for real-time ultrasound imaging within the heart chambers to guide interventional procedures.
The Foresight ICE System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Colibri Technologies, Inc. have in the registry?
The registry currently lists 1 device for Colibri Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Colibri Technologies, Inc.'s devices?
Among its 1 most recently registered device, Colibri Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Colibri Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Colibri Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Colibri Technologies, Inc. in the registry?
The most recently registered devices listed for Colibri Technologies, Inc. include Foresight Intracardiac Echocardiography (ICE) System.