Medical Device Manufacturer · US , St. Paul , MN

Exceleron Medical - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2014

Total

Cleared

Denied

Exceleron Medical has 2 FDA 510(k) cleared medical devices. Based in St. Paul, US.

Latest FDA clearance: Aug 2024. Active since 2014. Primary specialty: General Hospital.

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

510(k) submissions have been managed by ProMedic Consulting, LLC as regulatory consultant.

Exceleron Medical is one of 5134 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Exceleron Medical — FDA 510(k) Products and Clearance History

2 devices

1-2 of 2

Data Source

Sourced from the FDA 510(k) public files . 175,143 total devices indexed.

Last updated: May 11, 2026