Novocol, Inc. is one of 5108 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Novocol, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Novocol, Inc. has 9 FDA 510(k) cleared medical devices. Based in Louisville, US.
Historical record: 9 cleared submissions from 2004 to 2014. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Novocol, Inc. Filter by specialty or product code using the sidebar.
Novocol, Inc. — FDA 510(k) Products and Clearance History
9 devices
Cleared
Nov 14, 2014
BULK FILL FLOWABLE COMPOSITE
Dental
115d
Cleared
Oct 17, 2013
BIOROOT RCS
Dental
224d
Cleared
Dec 11, 2012
BPA-FREE MICROHYBID COMPOSITE
Dental
320d
Cleared
Jul 31, 2012
DIMER DUAL CURE PERMANENT/TEMPORARY RESIN CEMENT
Dental
182d
Cleared
May 21, 2012
ORTHODONTIC FLOWABLE BRACKET ADHESIVE
Dental
82d
Cleared
May 17, 2011
SELF CURE TEMPORARY CROWN AND BRIDGE MATERIAL
Dental
88d
Cleared
Nov 12, 2009
LIGHT-ACTIVATED LOW-STRESS THIOL-ENE COMPOSITE RESTORATIVE MATERIAL
Dental
90d
Cleared
Sep 13, 2007
DIMER ACID DERIVED NANO-HYBRID COMPOSITE RESTORATIVE MATERIAL
Dental
41d
Cleared
Aug 03, 2004
TEMP F
Dental
173d