Theodent, LLC - FDA 510(k) Cleared Devices

Theodent, LLC has 1 FDA 510(k) cleared medical devices. Based in New Orleans, US.

Latest FDA clearance: May 2025. Active since 2025. Primary specialty: Dental.

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

510(k) submissions have been managed by Blackwell Device Consulting as regulatory consultant.