Hemodia Sas - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Hemodia Sas has 4 FDA 510(k) cleared medical devices. Based in Labege, FR.
Last cleared in 2023. Active since 2013. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Hemodia Sas Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Visamed GmbH as regulatory consultant.
4 devices