Crospon, Ltd. is one of 12995 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Crospon, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: EndoFLIP System, EsoFLIP® ES-310 Balloon Catheter, EndoFLIP® System with FLIP Topography module
12
Total
12
Cleared
0
Denied
Crospon, Ltd. has 12 FDA 510(k) cleared gastroenterology & urology devices. Based in Bonita Springs, US.
Historical record: 12 cleared submissions from 2009 to 2019.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Crospon Ltd., C/O Promedic, LLC and Medtronic.
FDA 510(k) Regulatory Record - Crospon, Ltd.
12 devices
Cleared
Feb 15, 2019
EndoFLIP System
Gastroenterology & Urology
102d
Cleared
Nov 22, 2017
EsoFLIP® ES-310 Balloon Catheter
Gastroenterology & Urology
131d
Cleared
Apr 17, 2017
EndoFLIP® System with FLIP Topography module
Gastroenterology & Urology
28d
Cleared
May 01, 2016
EndoFLIP
Gastroenterology & Urology
46d
Cleared
Sep 25, 2014
ESOFLIP ES
Gastroenterology & Urology
64d
Cleared
Oct 07, 2013
ESOFLIP BALLOON DILATION CATHETER
Gastroenterology & Urology
73d
Cleared
Jul 17, 2013
ENDOFLIP CATHETER
Gastroenterology & Urology
107d
Cleared
Aug 27, 2012
BAROSTAT SOFTWARE OPTION
Gastroenterology & Urology
147d
Cleared
Oct 06, 2011
ENDOFLIP ECD
Gastroenterology & Urology
224d
Cleared
Jul 22, 2011
ENDOFLIP GASTRIC TUBE
Gastroenterology & Urology
148d
Cleared
Dec 16, 2010
ENDO FLIP
Gastroenterology & Urology
132d
Cleared
Dec 15, 2009
ENDOFLIP
Gastroenterology & Urology
90d