Medical Device Manufacturer · US , Westmont , IL

Immersivetouch - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2014

Total

Cleared

Denied

Immersivetouch has 3 FDA 510(k) cleared medical devices. Based in Westmont, US.

Last cleared in 2023. Active since 2014. Primary specialty: Radiology.

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

FDA 510(k) cleared devices by Immersivetouch

3 devices

1-3 of 3