Medical Device Manufacturer · BE , Namur

Sunrise SA - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2022

Total

Cleared

Denied

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) cleared devices by Sunrise SA

2 devices

1-2 of 2