Medinol, Ltd. - FDA 510(k) Cleared Devices
6
Total
3
Cleared
0
Denied
Medinol, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Tel-Aviv, IL.
Historical record: 3 cleared submissions from 1998 to 2018. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Medinol, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medinol, Ltd.
6 devices
Cleared
Jan 25, 2018
Gallant PTCA Dilatation Catheter
Cardiovascular
66d
Cleared
Jan 19, 2017
NC Gallant PTCA Catheter
Cardiovascular
141d
Cleared
Feb 12, 2016
X-Suit NIR Biliary Metallic Stent
Gastroenterology & Urology
352d
Cleared
Jan 09, 2009
MEDINOL X-SUIT NIR BILIARY METALLIC STENT
Gastroenterology & Urology
184d
Cleared
Oct 30, 2000
NIR BILIARY STENT
Gastroenterology & Urology
108d
Cleared
Nov 13, 1998
NIR BILIARY STENT
Gastroenterology & Urology
445d