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24 Oct 2018
Invibio
Press release

2nd International PEEK Meeting: Invibio Biomaterial Solutions spearheads medical research for implantable PEEK polymer devices
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Global meeting in Washington, D.C. puts spotlight on latest advances in the implementation of PEEK polymers for medical applications Thornton Cleveleys (UK) – Leading-edge research into medical-grade PEEK* technology and its clinical applications will be presented at the 2nd International PEEK [...]

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24 Oct 2018
Invibio MediTech HA receives FDA clearance
Press release

Invibio: Meditech Spine uses PEEK-OPTIMA™ HA Enhanced from Invibio for next generation of cervical intervertebral fusion devices
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Thornton Cleveleys (UK) – Meditech Spine, Atlanta/USA has received the US Food and Drug Administration (FDA) 510(k) clearance to market the next generation of its Talos™ line of interbody devices. These cervical intervertebral fusion devices rely on the novel implantable [...]

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24 Oct 2018
Invibio
Press release

Trauma technology platform from Invibio: a new metal-free solution for patients that may improve treatment
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New platform with clear device predicates in the US and Europe enables medical device manufacturers to expand their trauma offering beyond metal technologies Thornton Cleveleys (UK) – Medical device manufacturers looking to innovate and differentiate trauma products while delivering clinical benefits [...]

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24 Oct 2018
Invibio Osimplant HA
Press release

Invibio’s PEEK-OPTIMA™ HA Enhanced gains momentum: New Implant receives European approval
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Thornton Cleveleys (UK) – The next implants made from the PEEK-OPTIMA™ HA Enhanced implantable polymer have received the CE mark (European) approval. The CE mark is necessary for distributing products within the European Free Trade Association (EFTA) and the European [...]

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24 Oct 2018
Cervical cage HA
Press release

Invibio Biomaterial Solutions’ PEEK-OPTIMA™ HA Enhanced Receives First European Approval for Implant
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Thornton Cleveleys (UK) – Implants made from the PEEK-OPTIMA™ HA Enhanced implantable polymer have received their first CE mark (European) approval. It is granted to implants supplied by the Karmed Saglik Group (“Karmed”) for the treatment of degenerative spinal [...]

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