Corinth Medtech, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Corinth Medtech, Inc. has 7 FDA 510(k) cleared medical devices. Based in Cupertino, US.
Last cleared in 2023. Active since 2017. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Corinth Medtech, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Corinth Medtech, Inc.
7 devices
Cleared
Feb 24, 2023
Veloxion System
Gastroenterology & Urology
30d
Cleared
Jun 13, 2019
Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope,...
Gastroenterology & Urology
24d
Cleared
Jun 06, 2019
Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope,...
Obstetrics & Gynecology
20d
Cleared
Apr 24, 2019
Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope,...
Obstetrics & Gynecology
90d
Cleared
Mar 15, 2019
Veloxion Controller Kit, Veloxion Fluid Control Kit, Veloxion Resectoscope,...
Gastroenterology & Urology
52d
Cleared
Jul 25, 2018
Veloxion System, Veloxion Controller Kit, Veloxion Resecting Device Kit,...
Obstetrics & Gynecology
125d
Cleared
Mar 24, 2017
Veloxion System
Gastroenterology & Urology
149d