Medical Device Manufacturer · DK , Aarhus

Cercare Medical A/S - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2023

Total

Cleared

Denied

Cercare Medical A/S has 4 FDA 510(k) cleared medical devices. Based in Aarhus, DK.

Latest FDA clearance: Jun 2026. Active since 2023. Primary specialty: Radiology.

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

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

Cercare Medical A/S is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cercare Medical A/S

4 devices

1-4 of 4

Data Source

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

Last updated: Jul 06, 2026