Medical Device Manufacturer · FR , Paris

Gleamer Sas - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2025
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) cleared devices by Gleamer Sas

2 devices
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