Convatec, Ltd. is one of 174 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Convatec, Ltd. - FDA 510(k) Cleared Devices
4
Total
2
Cleared
0
Denied
Convatec, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Deeside, GB.
Historical record: 2 cleared submissions from 1997 to 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Convatec, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Convatec, Ltd.
4 devices
Cleared
Jul 21, 2015
Flexi-Seal Signal Fecal Management System
Gastroenterology & Urology
160d
Cleared
Aug 01, 2014
GENTLECATH MALE COUDE OLIVE TIP INTERMITTENT URINARY CATHETER
Gastroenterology & Urology
109d
Cleared
Dec 23, 1997
DUODERM CONTROL GEL FORMULA BORDER DRESSING
General & Plastic Surgery
88d
Cleared
Dec 23, 1997
DUODERM HYDROACTIVE DRESSING
General & Plastic Surgery
88d