Medical Device Manufacturer · US , Washington , DC

Jolife AB - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2006

Total

Cleared

Denied

Jolife AB has 5 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 5 cleared submissions from 2006 to 2018. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Jolife AB Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.

Jolife AB 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 - Jolife AB

5 devices

1-5 of 5

Data Source

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

Last updated: Jun 08, 2026