Amplify Surgical, Inc. - FDA 510(k) Cleared Devices

Amplify Surgical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Laguna Hills, US.

Last cleared in 2022. Active since 2019. Primary specialty: Orthopedic.

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

Regulatory submissions have been managed by Empirical Testing Corp and Empirical Technologies.