Whip-Mix Corp. is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Whip-Mix Corp. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Whip-Mix Corp. has 6 FDA 510(k) cleared medical devices. Based in Louisville, US.
Historical record: 6 cleared submissions from 2008 to 2014. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Whip-Mix Corp. Filter by specialty or product code using the sidebar.
Whip-Mix Corp. — FDA 510(k) Products and Clearance History
6 devices
Cleared
Sep 03, 2014
VERICORE ZIRCONIA BLANKS
Dental
149d
Cleared
Apr 29, 2014
COMFORTSOFT SOFT DENTURE LINER SYSTEM
Dental
97d
Cleared
Mar 26, 2014
WHIP MIX PREPPIES PLUS
Dental
282d
Cleared
Mar 04, 2010
VERICORE ABUTMENT IN TITANIUM FOR IMPLANT SYSTEMS
Dental
169d
Cleared
Jun 25, 2009
VERICORE ABUTMENT IN ZIRCONIA FOR IMPLANT SYSTEMS
Dental
80d
Cleared
Nov 20, 2008
VERICORE IMPLANT ABUTMENTS
Dental
100d