Curonix - FDA 510(k) Cleared Devices

Curonix has 1 FDA 510(k) cleared medical devices. Based in Pompano Beach, US.

Latest FDA clearance: Jun 2024. Active since 2024. Primary specialty: Neurology.

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

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