Medical Device Manufacturer · US , Houston , TX

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

2 submissions · 2 cleared · Since 2007

Total

Cleared

Denied

Endothelix, Inc. has 2 FDA 510(k) cleared medical devices. Based in Houston, US.

Historical record: 2 cleared submissions from 2007 to 2007. Primary specialty: Cardiovascular.

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

Endothelix, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

2 devices

1-2 of 2