Nexus Spine, LLC.

Also registered as Nexus Spine

Country not established FDA establishment FEI 3018210489

Devices: 19
Registrations: FDA
FDA recalls: 0

Catalogue19

Newest first, rows 1-19 of 19

Search and filter all 19 devices

DeltaNEC Interbody System Ref K261279

Class II

Active 510(k) 510(k) II
Tranquil Interbody System Ref K170297

Class II

Active 510(k) 510(k) II
Tranquil-L Interbody System Ref K233375

Class II

Active 510(k) 510(k) II
Stable-C Interbody System Ref K241467

Class II

Active 510(k) 510(k) II
PressON Spinal Fixation System Ref K253331

Class II

Active 510(k) 510(k) II
PressON Spinal Fixation System Ref K223529

Class II

Active 510(k) 510(k) II
Tranquil Interbody System Ref K181483

Class II

Active 510(k) 510(k) II
Tranquil-C Interbody System Ref K240416

Class II

Active 510(k) 510(k) II
Stable-L Standalone Lumbar Interbody System Ref K231486

Class II

Active 510(k) 510(k) II
Presson Spinal Fixation System Ref K133287

Class II

Active 510(k) 510(k) II
Stable-L Standalone Lumbar Interbody System, Stable-C Interbody System Ref K232530

Class II

Active 510(k) 510(k) II
Tranquil-L Interbody System Ref K181702

Class II

Active 510(k) 510(k) II
PressON Pro Spinal Fixation System Ref K160820

Class II

Active 510(k) 510(k) II
Stable-C Interbody System Ref K231763

Class II

Active 510(k) 510(k) II
Stable-L Lumbar Interbody System Ref K243934

Class II

Active 510(k) 510(k) II
Stable-L Standalone Lumbar Interbody System Ref K212498

Class II

Active 510(k) 510(k) II
PressON Spinal Fixation System Ref K233234

Class II

Active 510(k) 510(k) II
PreView-III™ Anterior Cervical Plate System Ref K223627

Class II

Active 510(k) 510(k) II
Stable-C Interbody System Ref K181621

Class II

Active 510(k) 510(k) II

Rows 1-19 of 19

Company details

FDA FEI number: 3018210489
Address: 4421 N Thanksgiving Way, Suite 101, Lehi, UT, 84043

Frequently asked questions

How many devices does NEXUS SPINE, LLC. have in the registry?

The registry currently lists 19 devices for NEXUS SPINE, LLC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list NEXUS SPINE, LLC.'s devices?

Among its 19 most recently registered devices, NEXUS SPINE, LLC. has devices listed in FDA 510(k) (19 devices).

What risk classes do NEXUS SPINE, LLC.'s devices fall under?

Among its 19 most recently registered devices, the classes recorded for NEXUS SPINE, LLC.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from NEXUS SPINE, LLC. in the registry?

The most recently registered devices listed for NEXUS SPINE, LLC. include DeltaNEC Interbody System, Tranquil Interbody System, Tranquil-L Interbody System and Stable-C Interbody System.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.

Catalogue19

DeltaNEC Interbody System Ref K261279

Tranquil Interbody System Ref K170297

Tranquil-L Interbody System Ref K233375

Stable-C Interbody System Ref K241467

PressON Spinal Fixation System Ref K253331

PressON Spinal Fixation System Ref K223529

Tranquil Interbody System Ref K181483

Tranquil-C Interbody System Ref K240416

Stable-L Standalone Lumbar Interbody System Ref K231486

Presson Spinal Fixation System Ref K133287

Stable-L Standalone Lumbar Interbody System, Stable-C Interbody System Ref K232530

Tranquil-L Interbody System Ref K181702

PressON Pro Spinal Fixation System Ref K160820

Stable-C Interbody System Ref K231763

Stable-L Lumbar Interbody System Ref K243934

Stable-L Standalone Lumbar Interbody System Ref K212498

PressON Spinal Fixation System Ref K233234

PreView-III™ Anterior Cervical Plate System Ref K223627

Stable-C Interbody System Ref K181621

Company details

Frequently asked questions