Medical Device Manufacturer · FR , Rennes

Therenva Sas - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2014
5
Total
5
Cleared
0
Denied

Therenva Sas has 5 FDA 510(k) cleared medical devices. Based in Rennes, FR.

Last cleared in 2022. Active since 2014. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Therenva Sas Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Therenva Sas

5 devices
1-5 of 5
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All5 Radiology 5