Bioserenity Sas - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Bioserenity Sas has 3 FDA 510(k) cleared medical devices. Based in Paris, FR.
Last cleared in 2023. Active since 2018. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Bioserenity Sas Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Bioserenity Sas
3 devices