Ice Neurosystems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ice Neurosystems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: iCE-SG2 Subcutaneous Electrode Kit, iCE-SG Subcutaneous Electrode Arrays, iCEWav Neuromonitoring Platform
3
Total
3
Cleared
0
Denied
Ice Neurosystems, Inc. has 3 FDA 510(k) cleared medical devices. Based in Washington, US.
Last cleared in 2022. Active since 2020. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Ice Neurosystems, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Eas Consulting Group, LLC, Acknowledge Regulatory Strategies, LLC and RQM+.
FDA 510(k) Regulatory Record - Ice Neurosystems, Inc.
3 devices