Additive Implants, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Additive Implants, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SureMAX-SA Cervical Standalone System, SureMAX Family of Cervical Spacers
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.
FDA 510(k) Regulatory Record - Additive Implants, Inc.
2 devices