Compremium AG - FDA 510(k) Cleared Devices

Compremium AG has 1 FDA 510(k) cleared medical devices. Based in Muri, CH.

Last cleared in 2023. Active since 2023. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Compremium AG Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Medidee Services, LLC as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.