Medical Device Manufacturer · FR , Pessac

Rebrain, Sas - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2023

Total

Cleared

Denied

Rebrain, Sas has 2 FDA 510(k) cleared medical devices. Based in Pessac, FR.

Latest FDA clearance: Aug 2024. Active since 2023. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Rebrain, Sas Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Rebrain, Sas

2 devices

1-2 of 2