Eminent Spine, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Eminent Spine, LLC - FDA 510(k) Cleared Devices
Recent clearances: Eminent Spine SI Screw System, Eminent Spine 3D Lumbar Interbody Fusion Systems, Cervical Stand-Alone System
4
Total
4
Cleared
0
Denied
Eminent Spine, LLC has 4 FDA 510(k) cleared medical devices. Based in Plano, US.
Latest FDA clearance: Jun 2024. Active since 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Eminent Spine, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Empirical Testing Corp, Eminent Spine and Jalex Medical.
FDA 510(k) Regulatory Record - Eminent Spine, LLC
4 devices