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Nexus Spine, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
18
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253331PressON Spinal Fixation SystemOctober 14, 2025
K243934Stable-L Lumbar Interbody SystemApril 30, 2025
K241467Stable-C Interbody SystemJuly 17, 2024
K233375Tranquil-L Interbody SystemMarch 20, 2024
K240416Tranquil-C Interbody SystemMarch 12, 2024
K233234PressON Spinal Fixation SystemOctober 26, 2023
K231486Stable-L Standalone Lumbar Interbody SystemOctober 12, 2023
K232530Stable-L Standalone Lumbar Interbody System, Stable-C Interbody SystemSeptember 18, 2023
K231763Stable-C Interbody SystemAugust 21, 2023
K223529PressON Spinal Fixation SystemMay 2, 2023
K223627PreView-III™ Anterior Cervical Plate SystemFebruary 2, 2023
K212498Stable-L Standalone Lumbar Interbody SystemMarch 18, 2022
K181621Stable-C Interbody SystemOctober 19, 2018
K181702Tranquil-L Interbody SystemSeptember 21, 2018
K181483Tranquil Interbody SystemAugust 27, 2018
K170297Tranquil Interbody SystemJune 27, 2017
K160820PressON Pro Spinal Fixation SystemJune 28, 2016
K133287PRESSON SPINAL FIXATION SYSTEMFebruary 25, 2014