Medical Device Manufacturer · US , San Francisco , CA

Cionic - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2022

Total

Cleared

Denied

Cionic has 2 FDA 510(k) cleared medical devices. Based in San Francisco, US.

Last cleared in 2022. Active since 2022. Primary specialty: Neurology.

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

FDA 510(k) cleared devices by Cionic

2 devices

1-2 of 2