Gleamer Sas is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Gleamer Sas - FDA 510(k) Cleared Devices
Recent clearances: ChestView US, BoneMetrics (US)
2
Total
2
Cleared
0
Denied
Gleamer Sas has 2 FDA 510(k) cleared medical devices. Based in Paris, FR.
Latest FDA clearance: Feb 2025. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Gleamer Sas Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gleamer Sas
2 devices