Djo, LLC - FDA 510(k) Cleared Devices

Djo, LLC has 13 FDA 510(k) cleared medical devices. Based in Vista, US.

Latest FDA clearance: Sep 2026. Active since 2009. Primary specialty: Physical Medicine.

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

510(k) submissions have been managed by Hogan Lovells Cadwalader US LLP as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.