Medical Device Manufacturer · US , North Reading , MA

Creagh Medical, Ltd. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2010

Total

Cleared

Denied

Creagh Medical, Ltd. has 5 FDA 510(k) cleared medical devices. Based in North Reading, US.

Last cleared in 2023. Active since 2010. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Creagh Medical, Ltd. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Dba Surmodics, Inc. as regulatory consultant.

Creagh Medical, Ltd. 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 - Creagh Medical, Ltd.

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: May 15, 2026