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

Curiteva, Inc. has 11 FDA 510(k) cleared orthopedic devices. Based in Tanner, US.

Latest FDA clearance: Jan 2026. Active since 2019.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Empirical Testing Corp and Mcra, LLC.