Hemcon Medical Technologies Europe, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hemcon Medical Technologies Europe, Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Hemcon Medical Technologies Europe, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Portland, US.
Historical record: 3 cleared submissions from 2010 to 2012. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Hemcon Medical Technologies Europe, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hemcon Medical Technologies Europe, Ltd.
3 devices
Cleared
Aug 21, 2012
GUARDIVA ANTIMICROBIAL HAEMSTATIC IV DRESSING
General & Plastic Surgery
95d
Cleared
Apr 12, 2012
HEMCON HEMOSTATIC GEL
General & Plastic Surgery
254d
Cleared
Jun 08, 2010
GUARDIVA ANTIMICROBIAL HAEMOSTATIC IV DRESSING, 1 IN/ 4MM, STERILE, GUARD IVA...
General & Plastic Surgery
187d