Life Spine

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
119
Inspections
5
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253748Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer SystemJanuary 23, 2026
K251502TruLift® Lateral Expandable Spacer & Lateral Buttress Plate SystemJuly 7, 2025
K250373ProLift Expandable Spacer SystemApril 9, 2025
K243668ProLift Pivot Expandable Spacer SystemJanuary 23, 2025
K243369Cervical Plating SystemDecember 11, 2024
K242826ProLift Wedge Expandable Spacer SystemOctober 8, 2024
K241464ARx® SAI Implant SystemJuly 29, 2024
K233455ARx MIS Spinal Screw SystemDecember 12, 2023
K232611TruLift Micro Expandable Spacer System & TruLift Expandable Spacer SystemNovember 30, 2023
K231704Pro-Link® & Pro-Link® Ti Barbs Cervical Spacer SystemOctober 19, 2023
K223430ProLift Micro Expandable Spacer SystemMay 4, 2023
K221806TruLift Lateral Expandable Spacer System & Lateral Plate SystemDecember 5, 2022
K222628Life Spine ALIF Buttress Plate SystemNovember 16, 2022
K213417Ghost Spacer SystemSeptember 29, 2022
K220341ARx Modular Spinal SystemMay 2, 2022
K220025ARx® Spinal SystemMarch 31, 2022
K212903SIMPACT Sacroiliac Joint Fixation SystemDecember 15, 2021
K212520ProLift Micro Expandable Spacer SystemOctober 8, 2021
K202836GX Navigation Instrument SystemAugust 19, 2021
K210061ProLift Lateral HELO FixatedApril 30, 2021