Life Spine

127 articles about Life Spine

• Life Spine Announces Continued Success and Portfolio Expansion With the PROLIFT® Expandable System

  12/8/2020

  Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced today the completion of multiple surgeries with the 8mm PROLIFT Expandable System.

• Life Spine Announces FDA 510(k) Clearance for SI Joint Revision Offering and Additional Claims for the SImpact® Sacroiliac Joint Fixation System

  9/22/2020

  Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced today that it has received clearance from the U.S. Food & Drug Administration (FDA) to market a SI revision offering and additional claims for the SImpact Sacroiliac Joint Fixation System. The new clearance adds a 14.5mm diameter screw to Life Spine’s SI fixation

• Life Spine Announces FDA 510(k) Clearance for the PLATEAU®-X Ti Lateral Lumbar Spacer System

  8/11/2020

  Life Spine Announces FDA 510(k) Clearance for the PLATEAU ® -X Ti Lateral Lumbar Spacer System

• Life Spine Announces FDA 510(k) Clearance for the PLATEAU®-A Ti Anterior Lumbar Spacer System

  8/5/2020

  Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced that it has received clearance from the U.S. Food & Drug Administration to market the PLATEAU-A Ti Anterior Lumbar Spacer System.

• Life Spine Announces Initiation of the PROLIFT® Lateral Expandable System Outcomes Study

  7/7/2020

  Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced today the initiation of the PROLIFT Lateral Expandable System prospective study.

• Life Spine Announces FDA 510(k) Clearance for Implant and Instrument Additions to the ARx® Spinal System for Adult Deformity

  4/28/2020

  Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced today that it has received clearance from the U.S. Food & Drug Administration (FDA) to market implant and instrument additions to the ARx Spinal System.

• Life Spine Announces FDA 510(k) Clearance of the PROLIFT® Lateral Fixated System

  4/21/2020

  Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced today that it has received clearance from the U.S. Food & Drug Administration (FDA) to market the PROLIFT Lateral Fixated System.

• Life Spine and Gizmo Medical Announce Production of Surgical Masks and Gowns to Meet Growing Demand

  3/23/2020

  Life Spine announced that in partnership with Gizmo Medical they are currently working on a production quantity of surgical masks and gowns and identifying ways to scale other medical equipment to meet the growing and urgent demand in the United States.

• Life Spine Grows Expandable Portfolio With Secondary FDA 510(k) of the Lateral PROLIFT® Expandable System and 20 New System Launches In 2020

  3/3/2020

  Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced today that it has received an additional clearance from the U.S. Food & Drug Administration (FDA) to market the Lateral PROLIFT Expandable System.

• Life Spine Announces FDA 510(k) of the Steerable PLATEAU® Ti System

  2/6/2020

  Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced that it has received clearance from the U.S. Food & Drug Administration to market the Steerable PLATEAU Ti System.

• Life Spine Releases White Paper on Immediate Restoration of Disc Height and Lordosis With PROLIFT® Expandable Spacer System

  1/28/2020

  Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced today that the Company has published a new white paper examining the immediate restoration of patient disc height, foraminal height and lordosis with the PROLIFT Expandable Spacer System.

• Life Spine Announces Significant Growth in 2019 Driven by Demand for Micro Invasive Technologies

  1/17/2020

  Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced today that the Company recognized significant growth across the business in 2019.

• Life Spine Announces FDA 510(k) Clearance of the Titanium Stand-Alone ALIF Spacer System

  12/23/2019

  Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced today that it has received clearance from the U.S. Food & Drug Administration (FDA) to market the Titanium Stand-Alone ALIF Spacer System.

• Life Spine Announces FDA 510(k) Clearance of the Award-winning LONGBOW® Titanium Lateral Expandable Spacer System

  11/21/2019

  Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced today that it has received clearance from the U.S. Food & Drug Administration (FDA) to market the LONGBOW Titanium Lateral Expandable Spacer System.

• Life Spine Announces First Cases With the CENTERLINE® Modular Thoracolumbar Spinal System

  11/19/2019

  Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced the initial surgeries of the CENTERLINE Modular Thoracolumbar Spinal System.

• Life Spine, Inc. is pleased to announce today that it has entered into a settlement agreement with the U.S. government that successfully resolves all of the government’s claims.

  11/8/2019

  Life Spine, Inc. is pleased to announce that it has entered into a settlement agreement with the U.S. government that successfully resolves all of the government’s claims.

• Life Spine Announces 510(k) Clearance of the Hinged Laminoplasty System

  9/26/2019

  Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced today the FDA 510(k) clearance of the Hinged Laminoplasty System.

• Life Spine Announces First Cases With the Micro Invasive PROLIFT® Lateral Expandable Spacer System

  9/24/2019

  Life Spine, a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders, announced the initial surgeries of the PROLIFT Lateral Expandable Spacer System.

• Life Spine Announces Expansion of International Sales to Thirty Countries Worldwide

  8/28/2019

  New customers in Vietnam and South America have recently begun purchasing products from Life Spine’s broad product portfolio and Life Spine has hosted over one hundred and forty international surgeons at cadaveric trainings since 2016.

• Life Spine Announces Initial Cases With Narrow Width Offerings of the PROLIFT® Expandable Spacer System

  8/20/2019

  The PROLIFT Expandable Spacer System is now available in width options from 8mm to 12mm and multiple height options that offer up to 6mm of continuous expansion.