Renerve, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Renerve, Ltd. has 1 FDA 510(k) cleared medical devices. Based in North Melbourne, AU.
Last cleared in 2022. Active since 2022. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Renerve, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Renerve, Ltd.
1 devices