Covalon Technologies, Ltd. is one of 16278 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
Recent clearances: ColActive Plus, COVAGEN, COLLAGRAN-COLLAGEN WOUND DRESSING, COLLAGRANAG-COLLAGEN W/SILVER ANTIMICROBIAL WOUND DRESSING
4
Total
4
Cleared
0
Denied
Covalon Technologies, Ltd. has 4 FDA 510(k) cleared medical devices. Based in Waxhaw, US.
Latest FDA clearance: Sep 2026. Active since 2006. 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.
FDA 510(k) Regulatory Record - Covalon Technologies, Ltd.
4 devices
Cleared
Sep 09, 2026
ColActive Plus
General & Plastic Surgery
194d
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