Ensi-Med International Pty. , Ltd. is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Ensi-Med International Pty. , Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Ensi-Med International Pty. , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Seaford, Victoria, AU.
Historical record: 1 cleared submissions from 2001 to 2001. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ensi-Med International Pty. , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ensi-Med International Pty. , Ltd.
1 devices