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Spine Fusion Devices Articles & Analysis

11 news found

Isto Biologics Launches Influx™ Fibrant, a New Line of Advanced Allograft

Isto Biologics Launches Influx™ Fibrant, a New Line of Advanced Allograft

Isto Biologics, a leader in surgical-based, orthobiologic regeneration technologies and cell-based therapies, announced today the launch of Influx™ Fibrant, an unprecedented line of functional constructs derived from 100% cortical allograft. The cutting-edge line consisting of five new products includes Fibrant Anchor, Boat, Bullet, Pak and Wrap. The Fibrant launch features the patented ...

ByIsto Biologics


Carlsmed Announces aprevo Launch and NTAP Reimbursement

Carlsmed Announces aprevo Launch and NTAP Reimbursement

” Starting today, spine fusion procedures utilizing Carlsmed’s aprevo® devices are eligible for additional reimbursement from CMS and private payors through the NTAP program. ...

ByCarlsmed, Inc.


Carlsmed aprevo Wins Spine Technology Award

Carlsmed aprevo Wins Spine Technology Award

” The aprevo® patient-specific interbody fusion devices are made possible by Carlsmed’s proprietary Data to Device™ digital technologies. ...

ByCarlsmed, Inc.


Locate Bio Closes £10 million Funding Round

Locate Bio Closes £10 million Funding Round

Funding to further advance Locate Bio’s regenerative medicine pipeline of orthobiologics Locate Bio, an orthobiologics focused regenerative medicine company, is pleased to announce that it has raised an oversubscribed £10 million of equity investment in a funding round co-led by existing shareholder Mercia Asset Management and new investor BGF. The funding will be used to further ...

ByLocate Bio Limited


Locate Bio’s Chondro3 Granted FDA Breakthrough Device Designation

Locate Bio’s Chondro3 Granted FDA Breakthrough Device Designation

The Company’s second FDA Breakthrough Device designation granted in 2021 Locate Bio, an orthobiologics focused regenerative medicine company, is pleased to announce that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Device designation to Chondro3, currently in development as a biomimetic graft for osteochondral lesions. The FDA Breakthrough Device Program is designed ...

ByLocate Bio Limited


CognitOss Granted FDA Breakthrough Device Designation

CognitOss Granted FDA Breakthrough Device Designation

FDA’s Breakthrough Device Program helps accelerate patient access to more effective treatments Locate Bio, an orthobiologics focused regenerative medicine company, is pleased to announce that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Device designation to CognitOss, currently in develoment for the treatment of chronic osteomyelitis. The FDA Breakthrough Device ...

ByLocate Bio Limited


Locate Bio appoints Keith Valentine as the Non-Executive Chair of the Board of Directors

Locate Bio appoints Keith Valentine as the Non-Executive Chair of the Board of Directors

Another important step towards its ambition of building a world leading, diversified orthobiologics company Locate Bio, an orthobiologics focused regenerative medicine company, is pleased to announce the appointment of Keith Valentine as the Non-Executive Chair of the Board with immediate effect. Keith joins with over 30 years’ experience in the orthopaedic industry, encompassing various ...

ByLocate Bio Limited


FDA Clears First Nanotechnology Peek Devices for Spinal Intervertebral Fusion

FDA Clears First Nanotechnology Peek Devices for Spinal Intervertebral Fusion

Exact same PEEK interbody device – only now, truly differentiated in the spine market with a PEEKplus® nanotexture. ...

ByExogenesis Corporation


Wenzel Spine Announces Acquisition of Statera Spine

Wenzel Spine Announces Acquisition of Statera Spine

Statera Spine is a software enabled spine imaging analytics company dedicated to providing easy-to-use solutions that facilitate improved care for patients suffering from chronic and acute spine issues. Standard pre-operative imaging does not allow for consideration of overall spine biomechanics, including sagittal alignment. The ...

ByWenzel Spine, Inc.


Ankasa Regenerative Therapeutics Receives $8.5 Million in First Tranche of $17 Million Series A Financing Led by Avalon Ventures

Ankasa Regenerative Therapeutics Receives $8.5 Million in First Tranche of $17 Million Series A Financing Led by Avalon Ventures

Ankasa Regenerative Therapeutics, Inc. (Ankasa), a company focused on pharmaceutical preparations for reactivation of stem cells for organ and tissue regrowth, tissue repair and healing, has received $8.5 million in the first tranche of a $17 million Series A round of financing led by La Jolla-based Avalon Ventures. Other participants in the financing include Heraeus Medical, a global business ...

ByAnkasa Regenerative Therapeutics


ASTM F2267 - 04(2011) Standard Test Method for Measuring Load Induced Subsidence of Intervertebral Body Fusion Device Under Static Axial Compression

ASTM F2267 - 04(2011) Standard Test Method for Measuring Load Induced Subsidence of Intervertebral Body Fusion Device Under Static Axial Compression

Intervertebral body fusion devices are generally simple geometric shaped devices, which are often porous or hollow in nature. Their function is to support the anterior column of the spine to facilitate arthrodesis of the motion segment. This test method is designed to quantify the subsidence characteristics ...

ByASTM International

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