Medical Device Manufacturer · IE , Galway

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

4 submissions · 4 cleared · Since 2018

Total

Cleared

Denied

Neuravi, Ltd. has 4 FDA 510(k) cleared medical devices. Based in Galway, IE.

Last cleared in 2021. Active since 2018. Primary specialty: Neurology.

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

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

Neuravi, Ltd. is one of 55 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Neuravi, Ltd.

4 devices

1-4 of 4

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: May 23, 2026