Medical Device Manufacturer · US , San Jose , CA

Corventis, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2009

Total

Cleared

Denied

Corventis, Inc. has 7 FDA 510(k) cleared medical devices. Based in San Jose, US.

Historical record: 7 cleared submissions from 2009 to 2014. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Corventis, Inc. Filter by specialty or product code using the sidebar.

Corventis, Inc. is one of 20575 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Corventis, Inc.

7 devices

1-7 of 7