Corinth Medtech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Corinth Medtech, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Veloxion System, Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch, Waste Management Bags, Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch, Waste Management Bags
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) Regulatory Record - 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