Medical Device Manufacturer · US , Wilmington , NC

Pjur Group Luxembourg S.A. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2014

Total

Cleared

Denied

Pjur Group Luxembourg S.A. has 6 FDA 510(k) cleared medical devices. Based in Wilmington, US.

Last cleared in 2021. Active since 2014. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Pjur Group Luxembourg S.A. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Candace F. Cederman as regulatory consultant.

FDA 510(k) Regulatory Record - Pjur Group Luxembourg S.A.

6 devices

1-6 of 6

Data Source

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

Last updated: May 22, 2026