Additive Implants, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Additive Implants, LLC - FDA 510(k) Cleared Devices
Recent clearances: Cervical Spacer
1
Total
1
Cleared
0
Denied
Additive Implants, LLC has 1 FDA 510(k) cleared medical devices. Based in Pheonix, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Additive Implants, LLC 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, LLC
1 devices