Xlumena, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Xlumena, Inc. - FDA 510(k) Cleared Devices
2
Total
1
Cleared
1
Denied
Xlumena, Inc. has 1 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Historical record: 1 cleared submissions from 2013 to 2014. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Xlumena, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Xlumena, Inc.
2 devices