Therapanacea Sas is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Therapanacea Sas - FDA 510(k) Cleared Devices
Recent clearances: ART-Plan+ (v3.1.0), ART-Plan+ (v.3.0.0), ART-Plan (v.2.2.0)
4
Total
4
Cleared
0
Denied
Therapanacea Sas has 4 FDA 510(k) cleared medical devices. Based in Paris, FR.
Latest FDA clearance: Dec 2025. Active since 2023. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Therapanacea Sas Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Therapanacea Sas
4 devices