Fasikl Incorporated is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fasikl Incorporated - FDA 510(k) Cleared Devices
Recent clearances: Felix NeuroAI System
1
Total
1
Cleared
0
Denied
Fasikl Incorporated has 1 FDA 510(k) cleared medical devices. Based in Bloomington, US.
Latest FDA clearance: Jul 2025. Active since 2025. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Fasikl Incorporated Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Fasikl Incorporated
1 devices