Cleerly, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cleerly, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Cleerly LABS (v2.0), Cleerly ISCHEMIA, Cleerly Labs v2.0
4
Total
4
Cleared
0
Denied
Cleerly, Inc. has 4 FDA 510(k) cleared medical devices. Based in New York, US.
Latest FDA clearance: Mar 2025. Active since 2019. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Cleerly, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Cleerly, Inc.
4 devices