Ventech Corp.
Country not established
- Devices
- 1
What Ventech Corp. makes
Ventech Corp. manufactures the VENTEX-IA, an intra-aortic balloon pump designed for temporary circulatory support in patients with acute heart failure or cardiogenic shock.
The VENTEX-IA 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
Ventex-Ia Ref K864641
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ventech Corp. have in the registry?
The registry currently lists 1 device for Ventech Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ventech Corp.'s devices?
Among its 1 most recently registered device, Ventech Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Ventech Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ventech Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ventech Corp. in the registry?
The most recently registered devices listed for Ventech Corp. include VENTEX-IA.