7
Total
7
Cleared
0
Denied

Pjur Group Luxembourg S.A. has 7 FDA 510(k) cleared medical devices. Based in Wilmington, US.

Latest FDA clearance: May 2026. 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.

7 devices
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