Nexus Spine, LLC - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Nexus Spine, LLC has 17 FDA 510(k) cleared orthopedic devices. Based in Salt Lake City, US.
Latest FDA clearance: Apr 2025. Active since 2014.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Nexus Spine, LLC
17 devices
Cleared
Apr 30, 2025
Stable-L Lumbar Interbody System
Orthopedic
131d
Cleared
Jul 17, 2024
Stable-C Interbody System
Orthopedic
55d
Cleared
Mar 20, 2024
Tranquil-L Interbody System
Orthopedic
170d
Cleared
Mar 12, 2024
Tranquil-C Interbody System
Orthopedic
29d
Cleared
Oct 26, 2023
PressON Spinal Fixation System
Orthopedic
28d
Cleared
Oct 12, 2023
Stable-L Standalone Lumbar Interbody System
Orthopedic
142d
Cleared
Sep 18, 2023
Stable-L Standalone Lumbar Interbody System, Stable-C Interbody System
Orthopedic
28d
Cleared
Aug 21, 2023
Stable-C Interbody System
Orthopedic
66d
Cleared
May 02, 2023
PressON Spinal Fixation System
Orthopedic
160d
Cleared
Feb 02, 2023
PreView-III™ Anterior Cervical Plate System
Orthopedic
59d
Cleared
Mar 18, 2022
Stable-L Standalone Lumbar Interbody System
Orthopedic
221d
Cleared
Oct 19, 2018
Stable-C Interbody System
Orthopedic
121d