Medical Device Manufacturer · IE , Galway

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

6 submissions · 6 cleared · Since 2020

Total

Cleared

Denied

Palliare , Ltd. has 6 FDA 510(k) cleared medical devices. Based in Galway, IE.

Latest FDA clearance: May 2024. Active since 2020. Primary specialty: Obstetrics & Gynecology.

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

Regulatory submissions have been managed by Palliare Ltd. C/O Promedic Consulting, LLC and ProMedic Consulting, LLC.

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

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: May 10, 2026