Erchonia Medical, Inc. - FDA 510(k) Cleared Devices

Erchonia Medical, Inc. has 10 FDA 510(k) cleared medical devices. Based in Littleton, US.

Historical record: 10 cleared submissions from 2004 to 2016. Primary specialty: Physical Medicine.

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

510(k) submissions have been managed by Regulatory Insight, Inc. as regulatory consultant. 2 devices have linked clinical trials registered on ClinicalTrials.gov.