Curio Digital Therapeutics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Curio Digital Therapeutics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MamaLift Plus
1
Total
1
Cleared
0
Denied
Curio Digital Therapeutics, Inc. has 1 FDA 510(k) cleared medical devices. Based in Princeton, US.
Latest FDA clearance: Apr 2024. Active since 2024. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Curio Digital Therapeutics, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Curio Digital Therapeutics, Inc.
1 devices