Celonova Biosciences, Inc. is one of 5631 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Celonova Biosciences, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Celonova Biosciences, Inc. has 5 FDA 510(k) cleared medical devices. Based in Newnan, US.
Historical record: 5 cleared submissions from 2008 to 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Celonova Biosciences, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Celonova Biosciences, Inc.
5 devices
Cleared
Aug 07, 2014
EMBOZENE COLOR-ADVANCED MICROSPHERES, EMBOZENE OPAQUE (NON-COLORED)...
Cardiovascular
90d
Cleared
Feb 24, 2014
EMBOZENE COLOR-ADVANCED MICROSPHERES, EMBOZENE OPAQUE (NON-COLORED) MICROSPHERES
Obstetrics & Gynecology
104d
Cleared
Oct 03, 2013
EMBOZENE MICROSPHERES
Cardiovascular
36d
Cleared
Mar 04, 2013
ONCOZENE MICROSPHERES 40UM, 2ML, ONCOZENE MICROSPHERES 75UM, 2ML, ONCOZENE...
Cardiovascular
25d
Cleared
Dec 15, 2008
EMBOZENE MICROSPHERES
Cardiovascular
377d