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19 devices found
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Manufacturer: Nexus Spine, LLC.
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Device · Manufacturer · Authorizations
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Class
DeltaNEC Interbody System
Nexus Spine, LLC.
·
,
FDA registration: United States
Class II
FDA 510(k)
K261279
Active
Cleared 22 Jun 2026
Active
510(k)
510(k)
II
Tranquil Interbody System
Nexus Spine, LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K170297
Active
Cleared 27 Jun 2017
Active
510(k)
510(k)
II
2 variants
Tranquil Interbody System
K181483
Tranquil-L Interbody System
Nexus Spine, LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K233375
Active
Cleared 20 Mar 2024
Active
510(k)
510(k)
II
2 variants
Tranquil-L Interbody System
K181702
Stable-C Interbody System
Nexus Spine, LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K241467
Active
Cleared 17 Jul 2024
Active
510(k)
510(k)
II
3 variants
Stable-C Interbody System
K181621
Stable-C Interbody System
K231763
PressON Spinal Fixation System
Nexus Spine
·
,
FDA registration: United States
Class II
FDA 510(k)
K253331
Active
Cleared 14 Oct 2025
Active
510(k)
510(k)
II
PressON Spinal Fixation System
Nexus Spine, LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K223529
Active
Cleared 2 May 2023
Active
510(k)
510(k)
II
3 variants
Presson Spinal Fixation System
K133287
PressON Spinal Fixation System
K233234
Tranquil-C Interbody System
Nexus Spine, LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K240416
Active
Cleared 12 Mar 2024
Active
510(k)
510(k)
II
Stable-L Standalone Lumbar Interbody System
Nexus Spine, LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K231486
Active
Cleared 12 Oct 2023
Active
510(k)
510(k)
II
2 variants
Stable-L Standalone Lumbar Interbody System
K212498
Stable-L Standalone Lumbar Interbody System, Stable-C Interbody System
Nexus Spine, LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K232530
Active
Cleared 18 Sep 2023
Active
510(k)
510(k)
II
PressON Pro Spinal Fixation System
Nexus Spine, LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K160820
Active
Cleared 28 Jun 2016
Active
510(k)
510(k)
II
Stable-L Lumbar Interbody System
Nexus Spine, LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K243934
Active
Cleared 30 Apr 2025
Active
510(k)
510(k)
II
PreView-III™ Anterior Cervical Plate System
Nexus Spine, LLC
·
,
FDA registration: United States
Class II
FDA 510(k)
K223627
Active
Cleared 2 Feb 2023
Active
510(k)
510(k)
II
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