Endogastric Solutions, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Endogastric Solutions, Inc. has 11 FDA 510(k) cleared gastroenterology & urology devices. Based in Redmond, US.
Latest FDA clearance: Apr 2024. Active since 2007.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
11 devices
Cleared
Apr 26, 2024
EsophyX Z+ Device with SerosaFuse Fasteners and Accessories
Gastroenterology & Urology
28d
Cleared
Oct 19, 2017
EsophyX Z, EsophyX2 HD
Gastroenterology & Urology
31d
Cleared
Jun 22, 2017
EsophyX2 HD Device with SerosaFuse Fasteners and Accessories, EsophyX Z...
Gastroenterology & Urology
50d
Cleared
May 01, 2016
EsophyX® Z Device with SerosaFuse Fasteners and Accessories
Gastroenterology & Urology
26d
Cleared
Mar 04, 2015
EsophyX® Z Fastener Delivery Device
Gastroenterology & Urology
72d
Cleared
Sep 30, 2014
ESOPHYX2 HD
Gastroenterology & Urology
57d
Cleared
Nov 06, 2009
ENDOGASTRIC SOLUTIONS ESOPHYX2 SYSTEM WITH SEROSAFUSE FASTENER AND...
Gastroenterology & Urology
92d
Cleared
Jul 22, 2009
ENDOGASTRIC SOLUTIONS STOMAPHYX SYSTEM WITH SEROSAFUSE FASTENER
Gastroenterology & Urology
30d
Cleared
Jun 27, 2008
ENDOGASTRIC SOLUTIONS STOMAPHYX DEVICE AND ACCESSORIES
Gastroenterology & Urology
184d
Cleared
Sep 14, 2007
EGS SEROSAFUSE IMPLANTABLE FASTENERS, ASSOCIATED DELIVERY DEVICES AND...
Gastroenterology & Urology
88d
Cleared
Mar 09, 2007
ENDOGASTRIC STOMAPHYX DEVICE AND ACCESSORIES
Gastroenterology & Urology
164d