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

Perfuze, Ltd. has 9 FDA 510(k) cleared medical devices. Based in Galway, IE.

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

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

1 device has linked clinical trial registered on ClinicalTrials.gov.