Life Spine, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SIMPACT Sacroiliac Joint Fixation System GX Navigation Instruments, VersaLift Expandable System, ARx® SAI Implant System
84
Total
84
Cleared
0
Denied
FDA 510(k) Regulatory Record - Life Spine, Inc. Orthopedic ✕
84 devices
Cleared
Jun 02, 2026
SIMPACT Sacroiliac Joint Fixation System GX Navigation Instruments
Orthopedic
103d
Cleared
May 12, 2026
VersaLift Expandable System
Orthopedic
60d
Cleared
Apr 16, 2026
ARx® SAI Implant System
Orthopedic
107d
Cleared
Jan 23, 2026
Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable...
Orthopedic
59d
Cleared
Jul 07, 2025
TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System
Orthopedic
53d
Cleared
Apr 09, 2025
ProLift Expandable Spacer System
Orthopedic
58d
Cleared
Jan 23, 2025
ProLift Pivot Expandable Spacer System
Orthopedic
57d
Cleared
Dec 11, 2024
Cervical Plating System
Orthopedic
42d
Cleared
Oct 08, 2024
ProLift Wedge Expandable Spacer System
Orthopedic
20d
Cleared
Jul 29, 2024
ARx® SAI Implant System
Orthopedic
67d
Cleared
Dec 12, 2023
ARx MIS Spinal Screw System
Orthopedic
53d
Cleared
Nov 30, 2023
TruLift Micro Expandable Spacer System & TruLift Expandable Spacer System
Orthopedic
94d
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