Minitube AB - FDA 510(k) Cleared Devices

Minitube AB has 1 FDA 510(k) cleared medical devices. Based in Tr?ngsviken, SE.

Last cleared in 2021. Active since 2021. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Minitube AB Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Mdi Consultants, Inc. as regulatory consultant.