Eminent Spine’s 3D Posterior In-Line Transfixing SI Joint System.
US-FDA 510 (K) clearance as of October 7, 2025.
Eminent Spine’s 3D Posterior In-Line Transfixing SI Joint System.
US-FDA 510 (K) clearance as of October 7, 2025.
Eminent Spine’s 3D Titanium Pedicle Screw System.
US-FDA 510(k) clearance as of April 28, 2025.
Eminent Spine’s Scoliosis Deformity Pedicle Screw System.
US-FDA 510(k) clearance as of August 20, 2024.
Eminent Spine’s 3D Titanium and Machined Titanium Si Screw System.
US-FDA 510(k) clearance as of June 4, 2024.
Eminent Spine’s 3D Titanium Lumbar Interbody Fusion Systems: PLIF/TLIF/ALIF.
US-FDA 510(k) clearance as of May 15, 2023.
Eminent Spine’s Cervical 3D Titanium cages are offered non-sterile.
US-FDA 510(k) clearance as of February 6, 2023.
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.
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.
Release of Surface Texture Pedicle Screw.
Released 4.75 mm Cannulated Pedicle Screw.
Release of C3 & S3 Pedicle Screw (tapered tip & thicker neck).
Release of 4.00mm MIS Pedicle Screw Towers & Instrumentation Delivery System.
Release of Grit Blasted Pedicle Rod with improved lordosis & marking.
US-FDA 510(k) Clearance for the modern, low-profile Anterior Cervical Plate System.
Lumbar and Cervical Peek IBFD System updated.
Lumbar Peek Lateral IBFD System updated.
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.
US-FDA 510(k) clearance for the anterior lumbar plating system.
Pedicle MIS System released.
Lumbar peek lateral cage system released.
International spinal sales begins.
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.
US-FDA 510(k) clearance for the cannulated & non-cannulated pedicle screw system & the lumbar cross-link.
US-FDA 510(k) clearance for the PEEK interbody fusion system.
US-FDA 510(k) clearance for the Anterior Lumbar Buttress System.
Eminent Spine was founded.
Eminent Spine is dedicated to manufacture biomechanically sound spinal implants and focus on surface technology.
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