Press Releases

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01 Feb 2018
Invibio Partnering with James Ellington
Press release

Invibio and Carbofix partnering with UK Olympic sprinter James Ellington on new “passion for progress” initiative
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Thornton Cleveleys (UK) – UK Olympic sprinter James Ellington has joined forces with the UK´s Invibio Biomaterial Solutions and CarboFix Orthopedics on his road to recovery and his overall ambition to return to the world stage of athletic competition after [...]

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24 Oct 2018
Surgeons learning advanced technology at CAOSNASS workshop
Press release

Invibio and Double Medical: Driving Implantable Devices using PEEK-OPTIMA™ into China
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Thornton Cleveleys (UK) – At the 10th Annual Congress of the Chinese Association of Orthopaedic Surgeons (CAOS), long-standing development partners Invibio Biomaterial Solutions, UK, and China’s Double Medical Technology Inc. ("Double Medical") collaborated on an interbody spine surgery workshop to [...]

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24 Oct 2018
Invibio
Press release

Invibio: Around 9 million implanted devices worldwide now using PEEK-OPTIMA™ polymer –“International PEEK meeting” upcoming
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Thornton Cleveleys (UK) – The number of implanted devices using PEEK-OPTIMA™ polymer has now increased to around nine million, worldwide. Pioneering developments and close collaboration with device companies, as well as assembling and sharing early clinical results with the medical [...]

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01 Feb 2018
Invibio Dental implant prosthetic framework
Press release

Further milestone for JUVORA dental disc: US FDA clears PEEK polymer CAD/CAM dental device for long-term implant borne prosthetics
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High performance polymer dental prosthetic device can potentially enable improved patient quality of life1 and efficiencies compared to metal. Thornton Cleveleys (UK) – A major innovation in dental prosthetics for comfort, durability and precision, the JUVORA™ dental disc, has received the US [...]

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01 Feb 2018
Posterior Spine Stablization
Press release

Invibio: FDA reclassified semi-rigid spinal stabilization systems providing new possibilities for treating patients
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Thornton Cleveleys (UK) – The US Food and Drug Administration (FDA) has recently reclassified semi-rigid spinal stabilization systems from Class III to Class II (*) offering a regulatory pathway to 510(k) clearance in the United States for innovative devices using [...]

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