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