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Eminent Spine

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
15
Inspections
4
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K250894Eminent Spine Posterior SI SystemOctober 7, 2025
K241663Eminent Spine 3D Titanium Pedicle Screw SystemApril 28, 2025
K242069Eminent Spine Scoliosis Deformity Pedicle Screw SystemSeptember 3, 2024
K240505Eminent Spine SI Screw SystemJune 4, 2024
K230219Eminent Spine 3D Lumbar Interbody Fusion SystemsMay 16, 2023
K212701Eminent Spine 3D Cervical Interbody Fusion SystemFebruary 6, 2023
K221936Standalone ALIF Interbody Fusion SystemOctober 17, 2022
K212853Cervical Stand-Alone SystemNovember 5, 2021
K201979Cervical Plate SystemAugust 25, 2020
K143365Eminent Foot Plate SystemMarch 30, 2015
K133194DIAMOND RATTLESNAKE SYSTEMJune 26, 2014
K103068KING COBRA ANTERIOR CERVICAL PLATEJanuary 14, 2011
K100377DIAMONDBACK SPINAL SYSTEMApril 22, 2010
K090415EMINENT SPINE BUTTRESS (FANG) PLATE SYSTEMJune 1, 2009
K090064EMINENT SPINE INTERBODY FUSION SYSTEMApril 9, 2009