Ziip, Inc. - FDA 510(k) Cleared Devices

Ziip, Inc. has 1 FDA 510(k) cleared medical devices. Based in Oakland, US.

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

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

510(k) submissions have been managed by Hill Regulatory Consulting, LLC as regulatory consultant.