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LG and Alienware monitors are Trojan horses, auto-installing Windows adware

LG and Alienware monitors silently install OEM apps and McAfee adware via Windows - here is how to stop it.

LG and Alienware monitors caught auto-installing Windows adware

Redditor "Mags_Smash" recently complained about seeing McAfee pop-up ads on his PC despite never having installed the ...
gadgets360

Alienware 15 Launched in India With Up to Ryzen 7 260 CPU, RTX 4050 GPU: Price, Specifications

Alienware 15 Launched in India With Up to Ryzen 7 260 CPU, RTX 4050 GPU: Price, Specifications Additional variants of Alienware 15 powered by Intel Core processors and Nvidia GeForce RTX 5060 GPUs ...
news.crunchbase

Crunchbase Data: Global Startup Investment Hit Record $510B In H1 2026 As AI Boom Accelerates Funding And Exits

Global venture funding reached a record $510 billion in the first half of 2026, surpassing the $440 billion invested in all of 2025 and setting a new high for startup investment in any half-year ...
FoneArena

Dell Alienware 15 gaming laptop with up to AMD Ryzen 7 260 CPU, RTX 4050 GPU launched in India

Dell Technologies and Alienware have launched the Alienware 15 in India. It is powered by AMD Ryzen 7 260 and Ryzen 5 220 processors, paired with NVIDIA GeForce RTX 3050 and RTX 4050 graphics, ...
360dx

BioMérieux Submits Updated Gastrointestinal Panels to FDA for 510(k) Review

NEW YORK – BioMérieux announced on Tuesday that it has submitted two gastrointestinal panels to the US Food and Drug Administration for 510(k) review. The BioFire FilmArray Gastrointestinal 1.1 Panel ...
Yahoo Finance

RefleXion Submits FDA 510(k) for Anchor Point Tracking, Advancing the Next Generation of SCINTIX Autonomous Radiotherapy

Anchor Point Tracking, designed for use with the new RefleXion X2 platform, underpins SCINTIX therapy with higher fidelity biologic data. "Anchor Point Tracking represents the next major advancement ...
MassDevice

Edwards picks up FDA nod for left atrial appendage clip

Edwards Lifesciences (NYSE:EW) has earned FDA 510(k) clearance for Ecliptis, its left atrial appendage (LAA) exclusion system. According to the FDA 510(k) database, the agency cleared the clip device ...
BioSpace

Life Spine Receives FDA 510(k) Clearance for VersaLift™ Expandable Interbody System Featuring a 6mm Starting Height

HUNTLEY, Ill.--(BUSINESS WIRE)--Life Spine, Inc., a medical device company that designs, develops, manufactures, and markets products for the surgical treatment of spinal disorders, announced today ...
Seeking Alpha

Conexeu Sciences: Hanging On The FDA 510(k) Pathway Submission

Conexeu Sciences is rated Buy, leveraging a patented CXU platform targeting multi-billion-dollar regenerative medicine markets with a flagship wound care product. CNXU’s Ten-Minute Tissue™ aims for ...
BioSpace

ECM Therapeutics Receives FDA 510(k) Clearance for ECMT-100 WMD

WARRENDALE, Pa., June 23, 2026 (GLOBE NEWSWIRE) -- ECM Therapeutics announced today that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance (K253521) for ECMT-100 WMD, a flowable ...
Business Wire

Pathway Labs Announces World's First FDA Clearance for Multicondition AI in Cardiology and Partnership with OpenEvidence

NEW YORK--(BUSINESS WIRE)--Pathway Labs today announced its public launch of EchoNext, the world’s first FDA-approved AI detection tool that reads standard 12-lead electrocardiograms (ECGs) to flag ...