Tag: Life Spine

Life Spine receives approval from FDA

Life Spine announces first surgical cases of ARx spinal fixation system

Life Spine has announced that the first surgical cases utilising its ARx spinal fixation system have been completed. According to Life Spine, the ARx spinal...
Life Spine receives approval from FDA

TruLift lateral expandable spacer system and lateral plate system granted FDA...

Life Spine has announced that it has received 510(k) clearance from the US Food and Drug Administration (FDA) to market its TruLift lateral expandable...
Life Spine receives approval from FDA

Life Spine announces first surgical cases of the ProLift micro endoscopic...

Life Spine has revealed the completion of the first surgical cases utilising its ProLift micro endoscopic expandable spacer system. ProLift micro is a uniquely designed...
Life Spine receives approval from FDA

Life Spine announces FDA 510(k) clearance for its GHOST 3D-printed titanium...

Life Spine has received clearance from the US Food and Drug Administration (FDA) to market the GHOST 3D-printed titanium spacer system, which includes new...
Life Spine receives approval from FDA

First surgical cases completed using Life Spine’s Dyna-Link titanium with barb...

Life Spine has announced that the first surgical cases using its Dyna-Link titanium device with barb fixation have been completed. The Dyna-Link titanium stand-alone...
Life Spine receives approval from FDA

Life Spine announces first surgical case of ProLift Lateral HELO fixated

Life Spine has announced the first surgical case of the ProLift Lateral HELO fixated expandable lateral spacer system. The ProLift Lateral HELO fixated with Osseo-Loc surface...
Life Spine receives approval from FDA

Life Spine receives FDA 510(k) clearance for ProLift micro expandable spacer...

Life Spine has received clearance from the US Food and Drug Administration (FDA) to market the ProLift micro Expandable Spacer System. ProLift micro is designed...
Life Spine receives approval from FDA

Life Spine completes first surgical cases with TRULIFT Expandable Spacer System

Life Spine has announced the completion of the first surgeries with the TRULIFT Expandable Spacer System–a micro-invasive technology for use in transforaminal lumbar interbody...
Life Spine receives approval from FDA

Life Spine announces FDA 510(k) clearance of the PROLIFT Lateral Fixated...

Life Spine has announced that it has received clearance from the US Food and Drug Administration (FDA) to market the PROLIFT Lateral Fixated system. “PROLIFT...
Life Spine receives approval from FDA

Life Spine to produce surgical masks during COVID-19 outbreak

Life Spine a medical device company that designs, develops, manufactures and markets products for the surgical treatment of spinal disorders has announced a partnership...
Life Spine receives approval from FDA

Life Spine receives US FDA 510(k) clearance for Steerable Plateau Ti...

Life Spine has announced that it has received 510(k) clearance from the US Food & Drug Administration (FDA) to market the Steerable Plateau Ti...

Life Spine publishes white paper on ProLift expandable spacer system

  Life Spine has announced today the publication of a white paper examining the immediate restoration of patient disc height, foraminal height and lordosis with...
Life Spine receives approval from FDA

Life Spine receives FDA 510(k) clearance for the titanium stand-alone ALIF...

Life Spine announced today that it has received clearance from the US Food and Drug Administration (FDA) to market the titanium stand-alone ALIF spacer...

Life Spine receives FDA 510(k) clearance for Longbow titanium lateral expandable...

Life Spine has received clearance from the US Food and Drug Administration (FDA) to market the Longbow titanium lateral expandable spacer system. The Longbow system...

Life Spine announces first cases with Centerline thoracolumbar spinal system

Life Spine has announced the initial surgeries using the Centerline modular thoracolumbar spinal system. The Centerline modular thoracolumbar spinal system features low profile 4.75mm cobalt...
Life Spine receives approval from FDA

Life Spine announces expansion of international sales to thirty countries worldwide

Life Spine recently announced that it is now selling its Micro Invasive suite of products in thirty countries worldwide. New customers in Vietnam and South...

FDA provides additional 510(k) clearance for the ProLift expandable spacer system

Life Spine announced today that the US Food and Drug Administration (FDA) has provided additional 510(k) market clearance for the ProLift expandable spacer system. “The...

Life Spine announces initiation of SIMPACT sacroiliac joint fixation outcomes study

Life Spine has announced the initiation of the SIMPACT sacroiliac joint (SI) fixation outcomes study, with Keith Maxwell of Southeastern Sports Medicine and Orthopedics...
Life Spine receives approval from FDA

Life Spine announces initiation of PROLIFT Expandable Interbody clinical study

Life Spine has announced the initiation of the PROLIFT Expandable clinical study with Ahmed Khan, Central Connecticut Neurosurgery and Spine, Connecticut, USA. Mariusz Knap, vice president...
Centerline

First robotically assisted surgeries with Centerline cortical screw and Prolift expandable spacer...

The first surgeries with robotically assisted minimally disruptive placement of the Centerline cortical screw system and the Prolift expandable spacer system (Life Spine) in...
Life Spine receives approval from FDA

Life Spine announces line extension of PRO-LINK titanium stand-alone cervical spacer...

The US Food and Drug Administration (FDA) has given 510(k) clearance to the PRO-LINK titanium stand-alone cervical spacer system (Life Spine) for spinal fusions. PRO-LINK...

First clinical use of SENTRY 2 lateral plating system announced by...

Life Spine, a privately held medical device company based in Huntley, Illinois, has announced the first clinical use of SENTRY 2 lateral plating system,...

Life Spine announces sales growth of ProLift Expandable Spacer System for...

Life Spine announced on 16 January that revenues for ProLift Expandable Spacer System grew by 493% for 2017 as compared to 2016. “With the...
Life Spine announces alpha release of the Sentry ALIF plating system

Rigid, low-profile design ALIF system receives alpha release

Life Spine have announced that their Sentry plating system, which has been designed to improve lumbar stabilisation in anterior lumbar interbody fusion (ALIF) procedures,...
Life Spine announces alpha release of the Sentry ALIF plating system

2 Rigid, low-profile design ALIF system receives alpha release

Life Spine have announced that their Sentry plating system, which has been designed to improve lumbar stabilisation in anterior lumbar interbody fusion (ALIF) procedures,...

First cases using multiple in-situ expansion methods performed with Life Spine’s...

The first cases have been performed with multiple methods of in-situ expansion using Life Spine’s product range. “Surgical intervention for the degenerative spine is a...

First clinical use of Life Spine’s TiBow expandable spacer system

Life Spine has announced the first clinical uses of its TiBow minimally invasive transforaminal lumbar interbody fusion (TLIF) expandable spacer system featuring Osseo-Loc surface...

Life Spine’s Prolift and Tibow spacers receive Osseo-Loc titanium surface treatment

Life Spine has announced the full commercial launch of two additions to the Osseo-Loc spinal implant range. The company’s ProLift expandable posterior/transforaminal lumbar interbody fusion...

Institutional review board approves Life Spine’s electrodiagnostic functional assessment study

A study to help determine outcomes for open vs. minimally invasive posterior lumbar spinal surgery has been approved by the Western Institutional Review Board....

Life Spine launches Prolift lordotic expandable interbody solution

Life Spine has announced the launch of its Prolift lordotic expandable interbody solution with the company’s Osseo-Loc technology. Prolift lordotic allows for in-situ disc height...

US FDA clears Life Spine’s Cranial Fusion system

The US Food and Drug Administration (FDA) has granted 510(k) clearance to Life Spine for its Cranial Fusion system. This clearance expands the indications...

US FDA clears Life Spine’s Plateau-C Ti cervical spacer system

The US Food and Drug Administration (FDA) has given 510(k) market clearance to Life Spine’s Plateau-C Ti cervical spacer system. The system utilises the company’s...

Life Spine introduces two new TLIF products at NASS 2016

Life Spine has introduced two new transforaminal lumbar interbody fusion (TLIF) products at the 2016 annual meeting of the North American Spine Society (NASS;...

Life Spine announces initial clinical cases with Pro-Link Ti stand-alone cervical...

Life Spine has successfully completed initial cases with its recently-launched Pro-Link Ti stand-alone cervical spacer system. Pro-Link Ti offers a low-profile, stand-alone cervical interbody,...

US FDA clears Life Spine’s Pro-Link Ti stand-alone cervical spacer system

Life Spine has announced that the US Food and Drug Administration (FDA) has given 510(k) marketing clearance to the company’s Pro-Link Ti stand-alone cervical...

Initial cases performed using Life Spine Sentry lateral plate system

Initial cases have been successfully completed with Life Spine’s Sentry lateral plate system. The product is designed to offer a low profile, intuitive design...