Vy Spine, LLC - FDA 510(k) Cleared Devices
Recent clearances: VyPlate™ Anterior Cervical Plate System, DiversiVy™ Facet Screw System, VyBrate™ VBR System
21
Total
21
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vy Spine, LLC Orthopedic ✕
21 devices
Cleared
Mar 27, 2026
VyPlate™ Anterior Cervical Plate System
Orthopedic
23d
Cleared
Mar 19, 2026
DiversiVy™ Facet Screw System
Orthopedic
169d
Cleared
Jan 07, 2026
VyBrate™ VBR System
Orthopedic
103d
Cleared
Mar 18, 2025
FortiVy™ OsteoVy™ Lumbar IBF
Orthopedic
271d
Cleared
Oct 16, 2024
Vy Spine™ VyLam™ Laminoplasty System
Orthopedic
30d
Cleared
Sep 24, 2024
LumiVy™ Lumbar IBF System
Orthopedic
300d
Cleared
Oct 30, 2023
ClariVy™ Cervical IBF System
Orthopedic
130d
Cleared
Oct 13, 2023
VyLink™ Spinal Screw System
Orthopedic
121d
Cleared
Oct 10, 2023
Vy Spine™ VyLam™ Laminoplasty System
Orthopedic
55d
Cleared
Sep 27, 2023
VySpan™ PCT System
Orthopedic
68d
Cleared
May 12, 2023
ClariVy™ Cervical IBF System
Orthopedic
85d
Cleared
Apr 18, 2023
UniVy™ OsteoVy™-Ti Cervical IBF System
Orthopedic
147d