Gynetech Pty. , Ltd. is one of 18423 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gynetech Pty. , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ManipulatOR PRO, ManipulatOR, InsufflatOR Needle, MANIPULATOR
4
Total
4
Cleared
0
Denied
Gynetech Pty. , Ltd. has 4 FDA 510(k) cleared medical devices. Based in Cincinnati, US.
Historical record: 4 cleared submissions from 2005 to 2015. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Gynetech Pty. , Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Macdonald Consulting and Quintiles Consulting.
FDA 510(k) Regulatory Record - Gynetech Pty. , Ltd.
4 devices