Corindus, Inc. - FDA 510(k) Cleared Devices

Corindus, Inc. has 9 FDA 510(k) cleared medical devices. Based in Baltimore, US.

Last cleared in 2022. Active since 2012. Primary specialty: Cardiovascular.

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

Regulatory submissions have been managed by Cardiomed Device Consultants and CardioMed Device Consultants, LLC. 2 devices have linked clinical trials registered on ClinicalTrials.gov.