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BioWorld - Tuesday, January 6, 2026
Home » Topics » Europe, BioWorld MedTech

Europe, BioWorld MedTech
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Reducer device

Neovasc touts NICE health tech assessment as a win

Nov. 24, 2021
By Mark McCarty
The U.K. National Institute of Health and Care Excellence (NICE) issued two health technology assessments dated Nov. 24, including one that gives a guarded recommendation for devices used to narrow the coronary sinus as a treatment for refractory angina. Neovasc Inc., of Richmond, British Columbia, touted the news as a positive for its Reducer device, given that this is the first instance in which NICE has lent any support for a device to treat the condition.
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Close-up of eye with digital focus

Pcube-Lab raises $4.75M to advance its eye-tracking technology

Nov. 24, 2021
By Bernard Banga
PARIS – Pcube-Lab BV has closed a $4.75 million funding round to deploy its eye tracking technology, Neuroclues, in Europe and the U.S. This technique helps with early diagnosis of neurological disorders such as Parkinson's, multiple sclerosis and Alzheimer's disease.
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Xeltis team members with a vessel device

European Investment Bank backs Xeltis’ restorative heart technology

Nov. 23, 2021
By Catherine Longworth
The European Investment Bank (EIB) pumped €15 million (US$17 million) into Xeltis BV to accelerate clinical programs for its polymer-based technology platform for cardiovascular restoration. The Eindhoven, Netherlands-based company is developing three types of cardiovascular implants. These are a pulmonary heart valve, coronary artery bypass graft and hemodialysis access grafts. The devices use a therapeutic approach called endogenous tissue restoration (ETR), which causes the patient’s own body to naturally restore a new blood valve. As the patient’s healing system develops a functional valve, Xeltis’ implant is gradually absorbed by the body.
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Brain illustration

Fujirebio Europe debuts two new Alzheimer’s disease biomarker tests

Nov. 22, 2021
By Catherine Longworth
Fujirebio Europe NV launched two new cerebrospinal fluid (CSF)-based immunoassays for Alzheimer’s Disease (AD) on its Innotest platform. It’s the first product launch for the company following a collaboration agreement signed with Adx Neurosciences NV in September 2020. The assays will test for neuronal pentraxin-2 (NPTX2) and soluble triggering receptor expressed on myeloid cells 2 (STREM2). Both neurology biomarkers are linked to synaptic dysfunction and neuroinflammation which are considered core features of AD progression. Fujirebio said the new tests will support existing research for AD drug development.
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British flag

COVID-19 hits UK’s research charities where it hurts: funding

Nov. 19, 2021
By Nuala Moran
LONDON – Medical research charities that form an integral part of the U.K. health research system are still reeling from the impact of COVID-19 and now expect it will be three years before funding returns to pre-pandemic levels.
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doctor, checklist, apple, prescription bottle and blood glucose meter illustration

Glyconics collects $2M for early diabetes screening tool

Nov. 19, 2021
By Catherine Longworth
Glyconics Ltd. landed £1.5 million (US$2 million) in an Enterprise Investment Scheme funding round to finance a clinical trial of its diabetes screening tool, Glyconics-SX. The Cambridge, U.K.-based diagnostics company is developing a point-of-care, hand-held device using miniaturized infrared (IR) spectrometry. The technology scans fingernails, assessing glycation to identify diabetes within minutes.
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Product image with microscopic close up

Istar reports first implants of Miniject glaucoma device after CE mark approval

Nov. 19, 2021
By Nuala Moran
LONDON – The first commercial implantations of Istar Medical SA’s minimally invasive Miniject supraciliary glaucoma drainage device have taken place in Germany, following European CE approval for the product.
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EU flags in front of the Berlaymont building

Surveillance of pre-MDR devices in EU to transition from legacy regulatory system

Nov. 18, 2021
By Mark McCarty
The European Union’s Medical Device Coordination Group (MDCG) continues to churn out guidances for the new Medical Device Regulations (MDRs), but there are several nagging questions about devices granted market access under the legacy system. MDCG has clarified that these devices will be subject to postmarket surveillance requirements under the MDR system rather than the previous system, although it is not a simple process to determine when this approach does and does not apply.
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Screenshot of ARVA software

Incepto develops deep learning solution to automate aortic aneurysm measurements

Nov. 17, 2021
By Bernard Banga
PARIS – Incepto Medical SAS, in partnership with Marie-Lannelongue Hospital, is developing an automated system to measure maximum aorta diameter. Called ARVA (Augmented Radiology for Vascular Aneurysm), it’s hosted in the cloud and is CE marked as a class I device. “Our tool uses the first algorithm to provide automatic measurement of external aortic diameter along the entire aorta, from ascending aorta to the iliac arteries,” Antoine Jomier, co-founder and CEO of Incepto, told BioWorld. This new tool for radiologists and surgeons will be used to diagnosis and monitor aneurysms.
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Stratasys 3D printers deployed at Hôpital Cochin

Bone 3D, Stratasys partner to deploy 3D printing across French hospitals

Nov. 16, 2021
By Bernard Banga
PARIS – Bone 3D SAS has signed a partnership with Stratasys Ltd. to put 3D printing technology directly into the hands of all 3,000 French hospitals and their front-line medical professionals. This new service, called Hospifactory, makes it possible to leverage additive manufacturing to produce medical equipment and devices directly on site at the hospital.
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