Medical Device Manufacturer · FR , Paris

Tissium SA - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 2025
2
Total
1
Cleared
1
Denied

Tissium SA has 1 FDA 510(k) cleared medical devices. Based in Paris, FR.

Latest FDA clearance: Sep 2025. Active since 2025. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Tissium SA Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Tissium SA

2 devices
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