Amplify Surgical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Amplify Surgical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DualXSLIM(R) T/PLIF, DualX, DualX Lumbar Intervertebral Body Fusion Device
3
Total
3
Cleared
0
Denied
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.
FDA 510(k) Regulatory Record - Amplify Surgical, Inc.
3 devices