Eminent Spine is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Eminent Spine - FDA 510(k) Cleared Devices
Recent clearances: Eminent Spine Posterior SI System, Eminent Spine 3D Titanium Pedicle Screw System, Eminent Spine Scoliosis Deformity Pedicle Screw System
11
Total
11
Cleared
0
Denied
Eminent Spine has 11 FDA 510(k) cleared orthopedic devices. Based in Leander, US.
Latest FDA clearance: Oct 2025. Active since 2009.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Jalex Medical as regulatory consultant.
FDA 510(k) Regulatory Record - Eminent Spine
11 devices
Cleared
Oct 07, 2025
Eminent Spine Posterior SI System
Orthopedic
196d
Cleared
Apr 28, 2025
Eminent Spine 3D Titanium Pedicle Screw System
Orthopedic
325d
Cleared
Sep 03, 2024
Eminent Spine Scoliosis Deformity Pedicle Screw System
Orthopedic
50d
Cleared
Feb 06, 2023
Eminent Spine 3D Cervical Interbody Fusion System
Orthopedic
530d
Cleared
Oct 17, 2022
Standalone ALIF Interbody Fusion System
Orthopedic
108d
Cleared
Mar 30, 2015
Eminent Foot Plate System
Orthopedic
126d
Cleared
Jun 26, 2014
DIAMOND RATTLESNAKE SYSTEM
Orthopedic
252d
Cleared
Jan 14, 2011
KING COBRA ANTERIOR CERVICAL PLATE
Orthopedic
88d
Cleared
Apr 22, 2010
DIAMONDBACK SPINAL SYSTEM
Orthopedic
69d
Cleared
Jun 01, 2009
EMINENT SPINE BUTTRESS (FANG) PLATE SYSTEM
Orthopedic
103d
Cleared
Apr 09, 2009
EMINENT SPINE INTERBODY FUSION SYSTEM
Orthopedic
90d