Medical Device Manufacturer · US , Washington , DC

Actegy , Ltd. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2013

Total

Cleared

Denied

Actegy , Ltd. has 7 FDA 510(k) cleared medical devices. Based in Washington, US.

Last cleared in 2021. Active since 2013. Primary specialty: Physical Medicine.

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

Regulatory submissions have been managed by The Allis Law Firm, Pllc, Hogan Lovells US LLP and Dohmen Life Science Services, LLC.

Actegy , Ltd. is one of 16081 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Actegy , Ltd.

7 devices

1-7 of 7

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: May 22, 2026