Therenva Sas is one of 271 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
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.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Therenva Sas
5 devices