Tournicare Pty, Ltd. is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Tournicare Pty, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Tournicare Pty, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Balwyn, AU.
Latest FDA clearance: Jun 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Tournicare Pty, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tournicare Pty, Ltd.
1 devices