Myohealth Technologies, LLC - FDA 510(k) Cleared Devices

Myohealth Technologies, LLC has 1 FDA 510(k) cleared medical devices. Based in Portland, US.

Latest FDA clearance: Feb 2024. Active since 2024. Primary specialty: Dental.

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

510(k) submissions have been managed by The Eyedeas Company as regulatory consultant.