Medical Device Manufacturer · US , Suite B , OR

Mecta Corporation - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2020

Total

Cleared

Denied

Mecta Corporation has 2 FDA 510(k) cleared medical devices. Based in Suite B, US.

Last cleared in 2021. Active since 2020. Primary specialty: Neurology.

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

FDA 510(k) cleared devices by Mecta Corporation

2 devices

1-2 of 2