Cionic is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cionic - FDA 510(k) Cleared Devices
Recent clearances: Cionic Neural Sleeve NS-100, Cionic Neural Sleeve NS-100
2
Total
2
Cleared
0
Denied
Cionic has 2 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Last cleared in 2022. Active since 2022. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Cionic Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cionic
2 devices