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BioWorld - Sunday, July 5, 2026
Home » Topics » Europe, Medical technology

Europe, Medical technology
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MHRA offers guidance on regulated, unregulated digital health apps

Feb. 4, 2025
By Mark McCarty
The U.K. Medicines and Health Care Products Regulatory Agency has provided guidance on what does and does not constitute a regulated digital mental health technology, but developers should be aware that promotional claims could push a product from the unregulated to the regulated category.
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C the Signs secures $8M for cancer prediction platform

Feb. 4, 2025
By Shani Alexander
C the Signs Ltd. recently received a capital injection of $8 million from Khosla Ventures to expand its AI-powered cancer prediction platform to the U.S. market.
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Hand cupping ear to illustration hearing loss

Essilorluxottica receives US, EU, green light for OTC Audio Glasses

Feb. 3, 2025
By Shani Alexander
Essilorluxottica SA received U.S. FDA clearance for its over-the-counter Nuance Audio Glasses, which combines sight and sound technologies, to help people improve their vision and hearing. The device also received a CE mark certification under the Medical Devices Regulation from the EU authorities.
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European Union flag with wooden gavel

MDCG lends clarity to the definition of an in vitro diagnostic

Feb. 3, 2025
By Mark McCarty
The EU’s Medical Device Coordination Group issued a guidance on the types of products that qualify as in vitro diagnostics (IVDs), including some important distinctions even in instances in which a given analyte is the subject of two tests.
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Cancer tumor in breast illustration

Tensive raises €14M for bio-absorbable breast implant

Jan. 31, 2025
By Shani Alexander
Tensive S.r.l. raised €14 million (US$14.5 million) in a series A financing round for its bio-absorbable breast implant Regenera, for patients undergoing reconstructive surgery after lumpectomy. The funds will be used to complete a pivotal clinical trial to evaluate the safety and performance of the technology.
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Gears with regulatory words

IMDRF mimics tri-agency approach to good machine learning practices

Jan. 31, 2025
By Mark McCarty
A new guidance by the International Medical Device Regulators Forum for good machine learning practices draws heavily on a 2021 playbook provided by Canada, the U.K. and the U.S., an outcome that also supports the notion that there is no point in reinventing a highly functional regulatory wheel.
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Stereotaxis robotic magnetic navigation (RMN) system

Stereotaxis begins anew with Genesisx launch in EU

Jan. 30, 2025
By Annette Boyle
Continuing a cascade of positive news for Stereotaxis Inc., the company reported the first order for its petite Genesisx robot in Europe. The system received CE mark in August, but management held off its launch until its Magic radiofrequency ablation catheter also received CE mark, which happened on Jan. 27. The two devices are used together to treat cardiac arrhythmias.
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Parkinson's disease illustration showing neurons containing alpha-synuclein

Neu Health secures $2M to bring platform to the US

Jan. 30, 2025
By Shani Alexander
Neu Health Ltd. received $2 million in funding from Cedars-Sinai Intellectual Property Company and Oxford Science Enterprises (OSE) to bring its platform, designed for Parkinson’s disease and dementia care, into the U.S.
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Artificial intelligence and digital health icons

EU trade associations call for withdrawal of AI Liability Directive

Jan. 30, 2025
By Mark McCarty
The EU has moved aggressively on legislation in recent years, with the AI Liability Directive serving as the latest example of legislation that sparked widespread opposition.
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Nobi Smart Light

Nobi raises €35M for smartlight to detect falls

Jan. 29, 2025
By Shani Alexander
Nobi BV secured €35 million (US$37 million) in an oversubscribed series B financing round to develop its artificial intelligence (AI)-powered smartlights which can detect falls in the elderly.
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