Lumen Biomedical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lumen Biomedical, Inc. - FDA 510(k) Cleared Devices
5
Total
4
Cleared
0
Denied
Lumen Biomedical, Inc. has 4 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Historical record: 4 cleared submissions from 2006 to 2011. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Lumen Biomedical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lumen Biomedical, Inc.
5 devices
Cleared
Aug 17, 2011
FIBERNET EMBOLIC PROTECTION DEVICE
Cardiovascular
35d
Cleared
Nov 18, 2008
FIBERNET EMBOLIC PROTECTION SYSTEM
Cardiovascular
95d
Cleared
Oct 02, 2008
LBI EMBOLECTOMY SYSTEM
Cardiovascular
185d
Cleared
Aug 10, 2007
XTRACT CATHETER SYSTEM
Cardiovascular
66d
Cleared
Jun 30, 2006
LBI CATHETER SYSTEM
Cardiovascular
207d