Corelink, LLC - FDA 510(k) Cleared Devices

Corelink, LLC has 35 FDA 510(k) cleared orthopedic devices. Based in Round Rock, US.

Last cleared in 2023. Active since 2008.

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 Technologies, Empirical Testing Corp and MCRA.