Medical Device Manufacturer · US , Miami Lakes , FL

Cordis US Corp - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2022

Total

Cleared

Denied

Cordis US Corp has 4 FDA 510(k) cleared medical devices. Based in Miami Lakes, US.

Latest FDA clearance: Jun 2024. Active since 2022. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Cordis US Corp Filter by specialty or product code using the sidebar.

Cordis US Corp 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 - Cordis US Corp

4 devices

1-4 of 4