Joimax GmbH - FDA 510(k) Cleared Devices

Joimax GmbH has 7 FDA 510(k) cleared medical devices. Based in Los Gatos, US.

Last cleared in 2021. Active since 2005. Primary specialty: Orthopedic.

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

510(k) submissions have been managed by Gary Mocnik and Associates as regulatory consultant.