Medical Device Manufacturer · US , Chicago , IL

Coapt - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2022

2

Total

2

Cleared

0

Denied

Coapt has 2 FDA 510(k) cleared medical devices. Based in Chicago, US.

Last cleared in 2023. Active since 2022. Primary specialty: Neurology.

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

FDA 510(k) cleared devices by Coapt

2 devices

1-2 of 2

Cleared Jan 11, 2023

Alpha Control Liner System (ACLS)

Neurology · 28d

Cleared Dec 30, 2022

ControlSeal Electrode (ELSB)

Neurology · 28d