Sim&Cure is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Sim&Cure has 6 FDA 510(k) cleared medical devices. Based in Grabels, FR.
Latest FDA clearance: Dec 2025. Active since 2019. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Sim&Cure Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medicept, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Sim&Cure
6 devices