Covalontechnologies, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Covalontechnologies, Inc. has 6 FDA 510(k) cleared medical devices. Based in Largo, US.
Historical record: 6 cleared submissions from 2005 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Covalontechnologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Covalontechnologies, Inc.
6 devices
Cleared
Sep 14, 2017
MediClear PreOp
General Hospital
269d
Cleared
Nov 24, 2015
SilverCoat Silicone Foley Catheter
Gastroenterology & Urology
266d
Cleared
Aug 13, 2012
SURGICLEAR ANTIMICROBIAL CLEAR SILICONE ADHESIVE DRESSING WITH CHLORHEXIDINE...
General & Plastic Surgery
53d
Cleared
May 04, 2012
IV CLEAR ANTIMICROBIAL CLEAR SILICONE ADHESIVE DRESSING WITH CHLORHEXIDINE...
General & Plastic Surgery
246d
Cleared
Jun 06, 2005
COLACTIVE AG COLLAGEN WITH SILVER ANTIMICROBIAL DRESSING
General & Plastic Surgery
189d
Cleared
Apr 27, 2005
COLACTIVE COLLAGEN WOUND DRESSING
General & Plastic Surgery
91d