Vy Spine, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
19
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253158VyBrate™ VBR SystemJanuary 7, 2026
K241783FortiVy™ OsteoVy™ Lumbar IBFMarch 18, 2025
K242784Vy Spine™ VyLam™ Laminoplasty SystemOctober 16, 2024
K233807LumiVy™ Lumbar IBF SystemSeptember 24, 2024
K231836ClariVy™ Cervical IBF SystemOctober 30, 2023
K231744VyLink™ Spinal Screw SystemOctober 13, 2023
K232471Vy Spine™ VyLam™ Laminoplasty SystemOctober 10, 2023
K232167VySpan™ PCT SystemSeptember 27, 2023
K230414ClariVy™ Cervical IBF SystemMay 12, 2023
K223513UniVy™ OsteoVy™-Ti Cervical IBF SystemApril 18, 2023
K223852VySpan™ PCT SystemFebruary 24, 2023
K223412LumiVy™ Lumbar IBF SystemJanuary 6, 2023
K221162UniVy OsteoVy Cervical IBF SystemNovember 4, 2022
K221572VyPlate Anterior Cervical Plate SystemJuly 26, 2022
K213750VyLink™ Spinal Screw SystemFebruary 28, 2022
K212930LumiVy Lumbar IBF SystemFebruary 16, 2022
K213219Vy Spine™ VyWasher™ Buttress SystemDecember 23, 2021
K212715Vy Spine ClariVy Cervical IBF SystemDecember 20, 2021
K213394Vy Spine™ VySpan™ PCT SystemDecember 10, 2021