Evolution Spine is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Evolution Spine - FDA 510(k) Cleared Devices
Recent clearances: E3D™-C Interbody System, Evolution Spine Navigation Instruments, E3D™-C Interbody System
8
Total
8
Cleared
0
Denied
Evolution Spine has 8 FDA 510(k) cleared medical devices. Based in Dallas, US.
Latest FDA clearance: Feb 2026. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Evolution Spine Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Evolution Spine
8 devices
Cleared
Feb 04, 2026
E3D™-C Interbody System
Orthopedic
29d
Cleared
Aug 18, 2025
Evolution Spine Navigation Instruments
Orthopedic
209d
Cleared
Aug 12, 2024
E3D™-C Interbody System
Orthopedic
47d
Cleared
May 15, 2024
E3D™-A Interbody System
Orthopedic
99d
Cleared
Jan 30, 2024
E3D™-A Interbody System
Orthopedic
172d
Cleared
Feb 07, 2023
EVOLUTION SPINE Interbody System
Orthopedic
125d
Cleared
Mar 18, 2022
EMERGE Anterior Cervical Plate System
Orthopedic
46d
Cleared
Sep 30, 2021
EMERGE™ Anterior Cervical Plate System
Orthopedic
59d