Medical Device Manufacturer · US , New York , NY

Cleerly, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2019

Total

Cleared

Denied

Cleerly, Inc. has 6 FDA 510(k) cleared medical devices. Based in New York, US.

Latest FDA clearance: Jul 2026. 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.

Cleerly, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cleerly, Inc.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 175,730 total devices indexed.

Last updated: Aug 06, 2026