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Sign in to claim this brandLife Spine, Inc.
US
Last updated September 17, 2026
What Life Spine, Inc. makes
Life Spine, Inc. manufactures spinal interbody fusion cages made from polymeric and metallic materials, including stand-alone and expandable designs for anterior and posterior lumbar applications. Their portfolio also includes non-bioabsorbable spinal fixation plates, screws, and rod-based internal fixation systems for stabilizing the spine. Additional products feature interspinous fixation implants, a reusable surgical retraction system, and cervical-specific devices such as stand-alone spacers and occipito-cervico-thoracic fixation systems.
The company’s devices are classified under FDA’s Class I, Class II, and Unclassified (U) categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Life Spine, Inc. manufacture?
Life Spine, Inc. specializes in spinal devices, primarily focusing on interbody fusion cages made from polymeric and metallic materials. These include stand-alone and expandable designs for both anterior and posterior lumbar applications. Their portfolio also covers non-bioabsorbable spinal fixation plates, screws, rod-based internal fixation systems, interspinous fixation implants, and reusable surgical retraction systems. Additionally, they produce cervical-specific devices like stand-alone spacers and occipito-cervico-thoracic fixation systems.
Where is Life Spine, Inc. based?
Life Spine, Inc. is headquartered in the United States. The company’s location is relevant for regulatory purposes, as it may influence compliance requirements and distribution networks for its devices.
Which regulatory registries or databases list Life Spine, Inc.’s devices?
Life Spine, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for healthcare providers, regulators, and other stakeholders by providing standardized identification for each device.
How are Life Spine, Inc.’s devices classified under FDA regulations?
Life Spine, Inc.’s devices fall under three FDA classification categories: Class I (generally low-risk devices), Class II (devices requiring special controls to ensure safety and effectiveness), and Unclassified (U) for devices that do not yet have a classification. The classification depends on factors like the device’s intended use, risk level, and regulatory history.
What is the significance of the device classifications for Life Spine, Inc.’s products?
The FDA classifications determine the regulatory pathway and scrutiny each device undergoes. Class I devices typically require less oversight, while Class II devices may need pre-market notifications (510(k)) or other submissions to demonstrate compliance with FDA requirements. Unclassified devices may require additional evaluation to assign an appropriate risk category before commercialization.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- 13951 Quality Dr, Huntley, IL, 60142
- Website
- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3004499989
- DUNS Number
- 183641617
Catalogue (9832)
Page 10 of 197| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| ProLift | 151-649 | FDA UDI | Class II | Active |
| Solstice Occipito-Cervico-Thoracic System | 9240-28 | FDA UDI | Class II | Active |
| Rogue | 154-468 | FDA UDI | Class II | Active |
| ProLift Wedge | L114-280-1 | FDA UDI | Class II | Active |
| Plateau A | 126-191 | FDA UDI | Class II | Active |
| Plateau V & Z | 129-753 | FDA UDI | Class II | Active |
| Plateau Spacer System | 51-1028-06 | FDA UDI | Class II | Active |
| Plateau Spacer System | 116-769 | FDA UDI | Class II | Active |
| Plateau Spacer System | 117-328 | FDA UDI | Class II | Active |
| Centric Plier Style Retractor | 149-1612 | FDA UDI | Class I | Active |
| Simpact | 152-08-640 | FDA UDI | Class II | Active |
| Plateau-C Ti | 36-1411-212 | FDA UDI | Class II | Active |
| Sentry Alif | 169-755-35 | FDA UDI | Class II | Active |
| Presidio Anterior Lumbar Fixation System | 125-50-38 | FDA UDI | Class II | Active |
| LONGBOW Spinal System | 149-869 | FDA UDI | Class II | Active |
| Plateau Ti Curved | 114-202-7 | FDA UDI | Class II | Active |
| Pilot Spinal System | 8400-140B | FDA UDI | Class II | Active |
| AVATAR Minimally Invasive Spinal System | 4550-095 | FDA UDI | Class II | Active |
| Plateau-C Spacer System | 36-1613-205 | FDA UDI | Class II | Active |
| Plateau A | 117-020 | FDA UDI | Class II | Active |
| Plateau Spacer System | 2014-0094 | FDA UDI | Class II | Active |
| Hammertoe (Rogue) | 154-479 | FDA UDI | Class II | Active |
| ProLift Trial | 151-423 | FDA UDI | Class II | Active |
| Foot and Ankle Plating System | 54-12S-10U | FDA UDI | Class II | Active |
| Plateau A | 116-981 | FDA UDI | Class II | Active |
| ALIF Disc Prep | 112-022 | FDA UDI | Class I | Active |
| Aileron Posterior Fusion System | 2012-0054 | FDA UDI | Class II | Active |
| Plateau Spacer System | 55-1031-08 | FDA UDI | Class II | Active |
| Dyna-Link Stand-Alone Anterior Lumbar System | 125-126 | FDA UDI | Class II | Active |
| Nautilus Spinal System | CAT45-40-5 | FDA UDI | Class II | Active |
| Nautilus | 112-280 | FDA UDI | Class II | Active |
| Aileron Posterior Fusion System | 132-510-2 | FDA UDI | Class II | Active |
| Simpact | 152-08-650 | FDA UDI | Class II | Active |
| Forefoot Screws | 20-2535 | FDA UDI | Class II | Active |
| Dyna-Link Stand-Alone Anterior Lumbar System | 80-3226-0615 | FDA UDI | Class II | Active |
| Plateau-C Spacer System | 36-1613-206 | FDA UDI | Class II | Active |
| ProLift Lateral | 151-1126 | FDA UDI | Class II | Active |
| Solstice Occipito-Cervico-Thoracic System | 117-896 | FDA UDI | Class II | Active |
| ProLift | 151-677 | FDA UDI | Class II | Active |
| Aileron Posterior Fusion System | 132-414-1 | FDA UDI | Class II | Active |
| Solstice Occipito-Cervico-Thoracic System | 9040-45 | FDA UDI | Class II | Active |
| Plateau Spacer System | 57-1027-11 | FDA UDI | Class II | Active |
| AVATAR Minimally Invasive Spinal System | 4551-125 | FDA UDI | Class II | Active |
| Plateau C | 113-757 | FDA UDI | Class II | Active |
| Plateau A | 117-062 | FDA UDI | Class II | Active |
| Modular Fixation System | NC050-050-4 | FDA UDI | Class II | Active |
| Nautilus | 114-517 | FDA UDI | Class II | Active |
| Plateau-X Spacer System | 2014-0128 | FDA UDI | Class II | Active |
| ProLift Trial | 151-398 | FDA UDI | Class II | Active |
| Foot and Ankle Plating System | 54-10T-20U | FDA UDI | Class II | Active |
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