Life Spine, Inc. - FDA 510(k) Cleared Devices
82
Total
82
Cleared
0
Denied
Life Spine, Inc. has 82 FDA 510(k) cleared orthopedic devices. Based in Hoffman Estates, US.
Latest FDA clearance: Apr 2026. Active since 2011.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Life Spine, Inc. as regulatory consultant.
82 devices
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
Cleared
Oct 19, 2023
Pro-Link® & Pro-Link® Ti Barbs Cervical Spacer System
Orthopedic
129d
Cleared
May 04, 2023
ProLift Micro Expandable Spacer System
Orthopedic
171d
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