Sunrise SA is one of 33 FDA 510(k) medical device manufacturers from Belgium in the dataset, ranked by real submission volume.
Sunrise SA has 2 FDA 510(k) cleared medical devices. Based in Namur, BE.
Latest FDA clearance: Aug 2025. Active since 2022. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Sunrise SA Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sunrise SA
2 devices