Data / Medical devices / United States / Life Spine
Life Spine: FDA-registered device maker in Huntley, IL, United States, 104 510(k) clearances
Life Spine is registered with the FDA (registration 3004499989) in Huntley, IL, United States. It lists 22 device types. The FDA files 104 510(k) clearances under its listings, the newest dated July 28, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004499989
- Address
- 13951 Quality Dr, Huntley, IL, United States, 60142
- Owner or operator
- LIFE SPINE (9061495)
- Roles
- Specification developer
- First device listed
- August 1, 2006
- Registered through
- 2026
- Brand names listed
- 2 hole plate, ALIF Buttress Plate, ARX, ARX SAI, ARx, ARx Modular, ARx SAI, Aileron and more
Devices it lists
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance. Newest 100 of 104.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 28, 2026 | K261430 | TruLift Expandable System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| June 2, 2026 | K260571 | SIMPACT Sacroiliac Joint Fixation System GX Navigation Instruments | OLO | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| May 12, 2026 | K260837 | VersaLift Expandable System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| April 16, 2026 | K254274 | ARx® SAI Implant System | NKB | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| January 23, 2026 | K253748 | Life Spine ProLift & ProLift Lateral and ProLift Lateral Fixated Expandable Spacer System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| April 9, 2025 | K250373 | ProLift Expandable Spacer System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| January 23, 2025 | K243668 | ProLift Pivot Expandable Spacer System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| December 11, 2024 | K243369 | Cervical Plating System | KWQ | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| October 8, 2024 | K242826 | ProLift Wedge Expandable Spacer System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| July 29, 2024 | K241464 | ARx® SAI Implant System | OUR | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| December 12, 2023 | K233455 | ARx MIS Spinal Screw System | NKB | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| November 30, 2023 | K232611 | TruLift Micro Expandable Spacer System & TruLift Expandable Spacer System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| October 19, 2023 | K231704 | Pro-Link® & Pro-Link® Ti Barbs Cervical Spacer System | OVE | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| May 4, 2023 | K223430 | ProLift Micro Expandable Spacer System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| December 5, 2022 | K221806 | TruLift Lateral Expandable Spacer System & Lateral Plate System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| November 16, 2022 | K222628 | Life Spine ALIF Buttress Plate System | KWQ | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| September 29, 2022 | K213417 | Ghost Spacer System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| May 2, 2022 | K220341 | ARx Modular Spinal System | NKB | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| December 15, 2021 | K212903 | SIMPACT Sacroiliac Joint Fixation System | OUR | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| October 8, 2021 | K212520 | ProLift Micro Expandable Spacer System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| August 19, 2021 | K202836 | GX Navigation Instrument System | OLO | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| April 30, 2021 | K210061 | ProLift Lateral HELO Fixated | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| April 22, 2021 | K210549 | ARx Spinal System | NKB | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| March 17, 2021 | K203361 | ProLift Wedge Expandable Spacer System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| December 17, 2020 | K203163 | ARx Illiac Spinal Screw System | NKB | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| September 18, 2020 | K201538 | Life Spine SIMPACT Sacroiliac Joint Fixation System | OUR | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| September 4, 2020 | K201721 | TruLift Expandable Spacer System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| August 4, 2020 | K201500 | Life Spine Plateau-A Ti Anterior Lumbar Spacer & Plateau-X Ti Lateral Lumbar Spacer | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| April 28, 2020 | K200896 | Solstice CCI | NKG | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| April 23, 2020 | K200070 | ARx Spinal System | NKB | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| April 17, 2020 | K200338 | ProLift Lateral Fixated | OVD | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| February 6, 2020 | K193521 | Steerable Plateau Ti | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| January 31, 2020 | K193258 | ProLift Expandable System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| December 16, 2019 | K191834 | Stand-Alone ALIF Titanium System | OVD | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| November 14, 2019 | K190721 | LongBow Ti | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| September 20, 2019 | K191927 | Hinged Laminoplasty System | NQW | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| August 8, 2019 | K191575 | ARx Spinal System | NKB | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| July 23, 2019 | K190488 | ProLift Expandable System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| June 13, 2019 | K191005 | ProLift® Expandable System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| March 13, 2019 | K183430 | Modular Spinal Fixation System | NKB | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| December 11, 2018 | K181625 | Life Spine Resolute Threaded Cage System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| November 26, 2018 | K182470 | Plateau Spacer System | MAX | Substantially Equivalent | Life Spine | accessdata.fda.gov |
| October 12, 2018 | K181717 | Life Spine Laminoplasty System | NQW | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| September 13, 2018 | K180215 | DYNA-LINK ELITE Stand-Alone Anterior Lumbar System | OVD | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| September 7, 2018 | K173883 | External Fixation System | KTT | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| June 22, 2018 | K180166 | Life Spine Lumbar Fixation System (SENTRY) | KWQ | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| June 15, 2018 | K180749 | Life Spine SIMPACT Sacroiliac Joint Fixation System | OUR | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| May 10, 2018 | K180642 | Pro-Link® Ti Stand-Alone Cervical Spacer System | OVE | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| February 2, 2018 | K172105 | The Plateau-LO Spacer System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| December 21, 2017 | K172973 | Life Spine Foot and Ankle Plating System | HRS | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| December 20, 2017 | K173182 | ProLift® Expandable System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| December 14, 2017 | K173286 | Cannulated Screw Internal Fixation System | HWC | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| August 28, 2017 | K172131 | 2 Hole Lateral Plating System | KWQ | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| August 3, 2017 | K170919 | The TiBow Expandable Spacer System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| July 7, 2017 | K171448 | Hammertoe Correction System | HWC | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| June 9, 2017 | K162685 | 2-Piece Hammertoe Correction System | HWC | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| May 18, 2017 | K170804 | The Solstice OCT System | NKG | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| May 1, 2017 | K162266 | The Cranial Fusion System | NKG | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| February 1, 2017 | K161279 | Life Spine Metatarsal Hemi Implant | KWD | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| December 22, 2016 | K161127 | The Small PLATEAU (PLATEAU-C) Spacer System | ODP | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| September 2, 2016 | K160066 | Pro-Link® Stand-Alone Cervical Spacer System | OVE | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| August 15, 2016 | K161037 | Tarsa-Link Stand-Alone Wedge Fixation System | HRS | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| August 1, 2016 | K153065 | The Hammertoe Correction System | HWC | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| June 23, 2016 | K160169 | The Life Spine Subtalar Implant System | HWC | Substantially Equivalent | Life Spine | accessdata.fda.gov |
| March 7, 2016 | K153400 | ProLift Expandable System | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| November 20, 2015 | K152282 | Cam Lock Plating System | KWQ | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| July 14, 2015 | K151196 | Nautilus Spinal System | NKB | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| July 7, 2015 | K151543 | Graft Delivery Device with Integrated Stylet | FMF | Substantially Equivalent | Micromedics, Inc. (D/B/A Nordson Medical) | accessdata.fda.gov |
| May 11, 2015 | K150126 | Life Spine Cannulated Screws | HWC | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| April 23, 2015 | K142253 | SOLSTICE OCT System | KWP | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| April 7, 2015 | K150229 | SOLSTICE OCT System | KWP | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| April 7, 2015 | K143249 | SOLSTICE OCT System | KWP | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| March 24, 2015 | K150368 | Tarsa-Link Wedge Fixation System | HRS | Substantially Equivalent | Life Spine | accessdata.fda.gov |
| March 16, 2015 | K150390 | Nautilus Spinal System | NKB | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| February 22, 2015 | K141246 | LIFE SPINE SACROILIAC JOINT FIXATION SYSTEM | OUR | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| February 12, 2015 | K141222 | NAUTILUS SPINAL SYSTEM AND SOLSTICE OCT SYSTEM | NKB | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| September 26, 2014 | K141905 | PRO-LINK WEDGE SYSTEM | HRS | Substantially Equivalent | Life Spine | accessdata.fda.gov |
| September 19, 2014 | K133717 | LONGBOW SPACER SYSTEM | MAX | Substantially Equivalent | Life Spine | accessdata.fda.gov |
| February 19, 2014 | K133564 | MODIFICATION TO NAUTILUS SPINAL SYSTEM | NKB | Substantially Equivalent | Life Spine, LLC | accessdata.fda.gov |
| October 28, 2013 | K132866 | NAUTILUS SPINAL SYSTEM | NKB | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| October 8, 2013 | K132589 | ANTERIOR LUMBAR PLATE SYSTEM (PRESIDIO) | KWQ | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| October 3, 2013 | K132760 | NAUTILUS SPINAL SYSTEM | NKB | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| June 13, 2013 | K130630 | PLATEAU SPACER SYSTEM TITANIUM | MAX | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| April 29, 2013 | K130202 | IRIS ANTERIOR CERVICAL PLATE | KWQ | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| March 6, 2013 | K123373 | NAUTILUS SPINAL SYSTEM | NKB | Substantially Equivalent | Life Spine | accessdata.fda.gov |
| November 16, 2012 | K121151 | PRO-LINK CERVICAL SPACER SYSTEM | OVE | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| October 1, 2012 | K120998 | SOLSTICE CROSS CONNECTOR | KWP | Substantially Equivalent | Life Spine | accessdata.fda.gov |
| August 7, 2012 | K111953 | NAUTILUS SPINAL SYSTEM | NKB | Substantially Equivalent | Life Spine | accessdata.fda.gov |
| May 8, 2012 | K121116 | PLATEAU SPACER SYSTEM | MAX | Substantially Equivalent | Life Spine | accessdata.fda.gov |
| March 13, 2012 | K113157 | AILERON INTERSPINOUS FIXATION SYSTEM | MNI | Substantially Equivalent | Life Spine | accessdata.fda.gov |
| September 7, 2011 | K111729 | PILOT SPINAL SYSTEM | NKB | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| July 19, 2011 | K111835 | PLATEAU SPACER SYSTEM | ODP | Substantially Equivalent | Life Spine, Inc. | accessdata.fda.gov |
| July 6, 2011 | K111569 | PLATEAU SPACER SYSTEM | MAX | Substantially Equivalent | Life Spine | accessdata.fda.gov |
| June 1, 2011 | K103423 | MIS ANTERIOR CERVICAL PLATING SYSTEM | KWQ | Substantially Equivalent | Life Spine | accessdata.fda.gov |
| November 5, 2010 | K100407 | LIFE SPINE INTERSPINOUS FIXATION SYSTEM | MNI | Substantially Equivalent | Life Spine | accessdata.fda.gov |
| October 13, 2010 | K093093 | SMALL PLATEAU SPACER SYSTEM | ODP | Substantially Equivalent | Life Spine | accessdata.fda.gov |
| January 19, 2010 | K093200 | LIFE SPINE LUMBAR PLATE SYSTEM | KWQ | Substantially Equivalent | Life Spine | accessdata.fda.gov |
| December 15, 2009 | K091301 | LIFE SPINE STAND-ALONE SPACER SYSTEM | OVD | Substantially Equivalent | Life Spine | accessdata.fda.gov |
| August 11, 2009 | K090343 | SENTINEL SPINAL SYSTEM | KWP | Substantially Equivalent | Life Spine | accessdata.fda.gov |
| January 28, 2009 | K083865 | PILOT SPINAL SYSTEM | MNI | Substantially Equivalent | Life Spine | accessdata.fda.gov |
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Updated July 28, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.