Phenox, Ltd. is one of 55 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Phenox, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Esperance pHLO Aspiration System, pNOVUS 21 Microcatheter, pNOVUS 21 Microcatheter
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.
FDA 510(k) Regulatory Record - Phenox, Ltd.
3 devices