Medical Device Manufacturer · FR , Labege

Hemodia Sas - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2013
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.

FDA 510(k) cleared devices by Hemodia Sas

4 devices
1-4 of 4
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All4 Orthopedic 4