Pjur Group Luxembourg S.A. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pjur Group Luxembourg S.A. - FDA 510(k) Cleared Devices
Recent clearances: pjur NATURE Touch, 100 ml, pjur WOMAN Aloe, pjur analyse me! water-based, pjur BACK DOOR water-based, pjur med Moisturising glide,pjur med NATURAL glide, We-Vibe Lube made by pjur, pjur AQUA Baseline, pjur AQUA Guarana, pjur AQUA ProVitamin B5, pjur BACK DOOR anal Provitamin B5
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.