Medical Device Manufacturer · IE , Galway

Phenox, Ltd. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2022
3
Total
3
Cleared
0
Denied

Phenox, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Galway, IE.

Latest FDA clearance: Jan 2026. Active since 2022. Primary specialty: Neurology.

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

FDA 510(k) cleared devices by Phenox, Ltd.

3 devices
1-3 of 3
Filters
All3 Neurology 3