Iotamotion, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Iotamotion, Inc. - FDA 510(k) Cleared Devices
Recent clearances: iotaSOFT® Insertion System
2
Total
1
Cleared
1
Denied
Iotamotion, Inc. has 1 FDA 510(k) cleared medical devices. Based in Iowa City, US.
Latest FDA clearance: Jan 2026. Active since 2021. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Iotamotion, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Darthur Consulting as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Iotamotion, Inc.
2 devices