Hemodia Sas is one of 273 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Hemodia Sas - FDA 510(k) Cleared Devices
Recent clearances: DOUBLEFLO INFLOW/OUTFLOW PUMP, accessories and tubing sets, DOUBLEFLO system, Zeos Aqua Vision Pump and tube
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.
Regulatory submissions have been managed by Visamed GmbH and Pharmalink Technical Group, LLC.
FDA 510(k) Regulatory Record - Hemodia Sas
4 devices