Insleep Technologies, LLC is one of 19127 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Insleep Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: Cloud9 System
1
Total
1
Cleared
0
Denied
Insleep Technologies, LLC has 1 FDA 510(k) cleared medical devices. Based in Eden Prairie, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Insleep Technologies, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Group as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Insleep Technologies, LLC
1 devices