Phenox, Ltd. - FDA 510(k) Cleared Devices
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.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
3 devices