Additive Implants, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Additive Implants, Inc. has 2 FDA 510(k) cleared medical devices. Based in Phoenix, US.
Last cleared in 2021. Active since 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Additive Implants, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Backroads Consulting as regulatory consultant.
2 devices