Curonix is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Curonix - FDA 510(k) Cleared Devices
Recent clearances: Freedom Peripheral Nerve Stimulator (PNS) System
1
Total
1
Cleared
0
Denied
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.
FDA 510(k) Regulatory Record - Curonix
1 devices