Penumbra, Inc. the world's leading thrombectomy company, announced it has secured CE Mark in Europe for THUNDERBOLT™, further laying the groundwork for launching computer assisted vacuum...

Induction Therapies, a leader in innovative skincare solutions and creator of the renowned Collagen P.I.N., announces their latest product, YouthXO + PDRN, a clean, recovery-and-renewal serum...

Alcon, the global leader in eye care dedicated to helping people see brilliantly, announced the launch and Canadian availability of UNITY® Cataract System (CS), Alcon’s next-generation standalone...

DermaSensor, a health technology company transforming skin cancer detection with AI-powered technology, announced it has received Class IIb CE Mark for the DermaSensor device, enabling...

ZEISS Medical Technology announced the successful early clinical implantations of the ZEISS AT LUCIA toric 721P intraocular lens (IOL), designed to treat cataracts while simultaneously correcting...

The New York Proton Center a global leader in proton therapy research and education and the first and only proton therapy center in New York, will share new research and clinical insights at the CID...

Sibel Health Inc., an award-winning medical technology company, announced that its ANNE® One system has received CE Mark certification under the European Union Medical Device Regulation (EU MDR...

Following the landmark first treatment at Stanford Medicine Cancer Center Care June 4, Leo Cancer Care announces the role of its Marie® upright patient positioning and imaging platform in enabling...

Igniton, a leader in emerging quantum wellness technologies, announced the launch of two new products: IgniREM Sleep™, a sleep-support formula designed to increase REM sleep which is important for...

Xenix Medical announced FDA 510(k) clearance and full commercial launch for its Lux Expandable Lumbar Interbody Fusion System.

A critically ill patient at Northwell’s North Shore University Hospital (NSUH) has been one of the first in the United States – and the first on the East Coast – to successfully be treated with an...

Waters Corporation announced that the BD BACTEC FXI Culture System has received U.S. Food and Drug Administration (FDA) 510(k) clearance.