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Sign in to claim this brandLife Spine, Inc.
US
Last updated September 17, 2026
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 1 of 197| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nautilus Spinal System | TNC55-55-5 | FDA UDI | Class II | Active |
| Aileron Posterior Fusion System | 132-1-100 | FDA UDI | Class II | Active |
| Nautilus Spinal System | 114-184 | FDA UDI | Class II | Active |
| Dyna-Link Stand-Alone Anterior Lumbar System | 77-3428-611 | FDA UDI | Class II | Active |
| Plateau-LO Spacer System | 46-1036-711 | FDA UDI | Class II | Active |
| Resolute | 129-1256 | FDA UDI | Class II | Active |
| Nautilus Spinal System | 148-513 | FDA UDI | Class II | Active |
| Nautilus Spinal System | 148-117 | FDA UDI | Class II | Active |
| Solstice Occipito-Cervico-Thoracic System | 9435-14 | FDA UDI | Class II | Active |
| Hinged Laminoplasty | 174-812PM | FDA UDI | Class II | Active |
| ProLift | 149-2124 | FDA UDI | Class II | Active |
| Pro-Link Stand-Alone Cervical Spacer System | 2014-0151 | FDA UDI | Class II | Active |
| Plateau Spacer System | 52-1024-15 | FDA UDI | Class II | Active |
| Gruve Anterior Cervical Plate System | 153-014 | FDA UDI | Class II | Active |
| Nautilus | 2019-0078 | FDA UDI | Class II | Active |
| Arx | 16-7590-13 | FDA UDI | Class II | Active |
| Dyna-Link Stand-Alone Anterior Lumbar System | 125-961 | FDA UDI | Class II | Active |
| Solstice Occipito-Cervico-Thoracic System | 3250-070 | FDA UDI | Class II | Active |
| Pilot Spinal System | 8400-075B | FDA UDI | Class II | Active |
| Plateau-C Ti | 55-1034-0714T | FDA UDI | Class II | Active |
| Centric - T Retractor | 149-1603 | FDA UDI | Class I | Active |
| Nautilus Spinal System | 375-45-5 | FDA UDI | Class II | Active |
| ProLift Expandable Spacer System | 2018-0026 | FDA UDI | Class II | Active |
| Pilot Spinal System | 2012-0077 | FDA UDI | Class II | Active |
| NEO UL Anterior Cervical Plate System | 328-016 | FDA UDI | Class II | Active |
| Dyna-Link Ti | L148-402 | FDA UDI | Class II | Active |
| Plateau Spacer System | 40-1020-711 | FDA UDI | Class II | Active |
| ProLift Micro | 58-0832-0708M | FDA UDI | Class II | Active |
| Foot and Ankle Plating System | 154-350 | FDA UDI | Class II | Active |
| Plateau Lo | 129-1301 | FDA UDI | Class II | Active |
| Prolift Post-Pack Instruments | 151-295 | FDA UDI | Class II | Active |
| Solstice Occipito-Cervico-Thoracic System | 9255-17 | FDA UDI | Class II | Active |
| Plateau-X Spacer System | 86-2245-013 | FDA UDI | Class II | Active |
| Pilot Spinal System | 113-323 | FDA UDI | Class II | Active |
| Centerline | 148-234 | FDA UDI | Class II | Active |
| Hinged Laminoplasty | 174-812HM | FDA UDI | Class II | Active |
| Centerline Thoracolumbar Spinal System | 4075-85-41 | FDA UDI | Class II | Active |
| Plateau Spacer System | 54-1024-710 | FDA UDI | Class II | Active |
| Plateau-C Ti | 22-1613-14T | FDA UDI | Class II | Active |
| Plateau Spacer System | 2014-0087 | FDA UDI | Class II | Active |
| Nautilus Spinal System | 755-35-5 | FDA UDI | Class II | Active |
| ProLift Lateral | 151-1078 | FDA UDI | Class II | Active |
| Hinged Laminoplasty | 174-910MM | FDA UDI | Class II | Active |
| ProLift Lateral Fixated | 58-2245-1513LP | FDA UDI | Class II | Active |
| Centerline Cannulated Accessories | 6875-070 | FDA UDI | Class II | Active |
| Plateau-C Ti | 113-992 | FDA UDI | Class II | Active |
| Nautilus | 148-136 | FDA UDI | Class II | Active |
| Nautilus Spinal System | TNC45-45-5 | FDA UDI | Class II | Active |
| Foot and Ankle Plating System | 54-04T-2800R | FDA UDI | Class II | Active |
| ALIF Disc Prep | 114-310 | FDA UDI | Class I | Active |
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