Timeline Of Eminent Spine

  • October 2025

    3d Posterior Inline Transfixing Si Joint System Image

    Eminent Spine’s 3D Posterior In-Line Transfixing SI Joint System.

    US-FDA 510 (K) clearance as of October 7, 2025.

  • Es Timeline 1 Revise 1

    Eminent Spine’s 3D Titanium Pedicle Screw System.

    US-FDA 510(k) clearance as of April 28, 2025.

    April 2025

  • August 2024

    Es Timeline 2

    Eminent Spine’s Scoliosis Deformity Pedicle Screw System.

    US-FDA 510(k) clearance as of August 20, 2024.

  • Es Timeline 3

    Eminent Spine’s 3D Titanium and Machined Titanium Si Screw System.

    US-FDA 510(k) clearance as of June 4, 2024.

    June 2024

  • May 2023

    Es Timeline 4

    Eminent Spine’s 3D Titanium Lumbar Interbody Fusion Systems: PLIF/TLIF/ALIF.

    US-FDA 510(k) clearance as of May 15, 2023.

  • Es Timeline 5

    Eminent Spine’s Cervical 3D Titanium cages are offered non-sterile.

    US-FDA 510(k) clearance as of February 6, 2023.

    February 2023

  • October 2022

    Es Timeline 6

    Eminent Spine’s Lumbar Stand-Alone System includes non-sterile implants with 5 implant profiles and hyperlordotic angles.

    Lumbar PEEK & 3d Titanium Cages are available in our Stand-Alone System.

    US-FDA 510(k) clearance as of October 17, 2022.

  • Es Timeline 7

    Eminent Spine’s Cervical Stand-Alone System includes non-sterile implants with a wide range of implant profiles with both Fixed and Variable Screw Options.

    Cervical Peek, Titanium & 3D Ti Cages are offered in our Stand-Alone System.

    US-FDA 510(k) clearance as of November 5, 2021.

    November 2021

  • January 2021

    Es Timeline 8

    Release of Surface Texture Pedicle Screw.

    Released 4.75 mm Cannulated Pedicle Screw.

  • Es Timeline 9 1

    Release of C3 & S3 Pedicle Screw (tapered tip & thicker neck).

    Es Timeline 9 2

    Release of 4.00mm MIS Pedicle Screw Towers & Instrumentation Delivery System.

    Release of Grit Blasted Pedicle Rod with improved lordosis & marking.

    November 2020

  • October 2020

    Es Timeline 10

    US-FDA 510(k) Clearance for the modern, low-profile Anterior Cervical Plate System.

  • Es Timeline 11 1

    Lumbar and Cervical Peek IBFD System updated.

    Es Timeline 11 2

    Lumbar Peek Lateral IBFD System updated.

    June 2020

  • February 2020

    Es Timeline 12

    Eminent Spine underwent full transformation including rebranding, administration changes and new FDA clearances.

    Relocated to new headquarters in Plano, TX.

  • US-FDA 510(k) clearance for eminent extremities.

    2015

  • 2014

    US-FDA 510(k) clearance for the anterior lumbar plating system.

  • Es Timeline 13 1

    Pedicle MIS System released.

    Es Timeline 13 2

    Lumbar peek lateral cage system released.

    2013

  • 2012

    International spinal sales begins.

  • Es Timeline 14

    US-FDA 510(k) clearance for the anterior cervical plating system.

    Eminent Spine releases the anterior cervical plate clinical data.

    Eminent Spine releases the lumbar pedicle screw & cross-link clinical data.

    2011

  • 2010

    Es Timeline 15

    US-FDA 510(k) clearance for the cannulated & non-cannulated pedicle screw system & the lumbar cross-link.

  • Es Timeline 16 1

    US-FDA 510(k) clearance for the PEEK interbody fusion system.

    Es Timeline 16 2

    US-FDA 510(k) clearance for the Anterior Lumbar Buttress System.

    2009

  • 2008

    Eminent Spine was founded.

Eminent Spine

Eminent Spine is dedicated to manufacture biomechanically sound spinal implants and focus on surface technology.

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