Medical Device Manufacturer · US , Laguna Hills , CA

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

3 submissions · 3 cleared · Since 2019

Total

Cleared

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.

FDA 510(k) cleared devices by Amplify Surgical, Inc.

3 devices

1-3 of 3