Immersivetouch is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Immersivetouch - FDA 510(k) Cleared Devices
Recent clearances: Ikshana, ImmersiveView Surgical Plan (IVSP®)
3
Total
3
Cleared
0
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) Regulatory Record - Immersivetouch
3 devices