Nanovis Spine, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nanovis Spine, LLC - FDA 510(k) Cleared Devices
Recent clearances: Nano FortiFix® System
3
Total
3
Cleared
0
Denied
Nanovis Spine, LLC has 3 FDA 510(k) cleared medical devices. Based in Columbia City, US.
Historical record: 3 cleared submissions from 2015 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Nanovis Spine, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Backroads Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Nanovis Spine, LLC
3 devices