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.

Rebrain, Sas is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Rebrain, Sas

2 devices

1-2 of 2