Covalon Technologies, Ltd. is one of 5180 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Covalon Technologies, Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Covalon Technologies, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Waxhaw, US.
Historical record: 3 cleared submissions from 2006 to 2013. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Covalon Technologies, Ltd. Filter by specialty or product code using the sidebar.
Covalon Technologies, Ltd. — FDA 510(k) Products and Clearance History
3 devices
Cleared
Aug 16, 2013
COVAGEN
General & Plastic Surgery
252d
Cleared
Apr 18, 2006
COLLAGRAN-COLLAGEN WOUND DRESSING, COLLAGRANAG-COLLAGEN W/SILVER...
General & Plastic Surgery
25d
Cleared
Feb 03, 2006
COVACLEARAG COLLAGEN WITH SILVER ANTIMICROBIAL GEL SHEET DRESSING
General & Plastic Surgery
128d