Arkose Labs today announced the launch of Arkose Device ID, a device identification solution that combines precise device tracking with session-based risk signals and anti-spoofing technology. Arkose ...

The most recent meeting of the International Medical Device Regulators Forum (IMDRF), the regulators-only successor group to the Global Harmonization Task Force (GHTF), indicates that the organization ...

SAN MATEO, Calif.--(BUSINESS WIRE)--Arkose Labs, the leading proactive fraud deterrence provider, today announced the latest release of Arkose Device ID, a solution within the new Arkose Titan™ ...

In a highly anticipated move, the US Food and Drug Administration (FDA) has announced the final release of the Unique Device Identification (UDI) rule, reflecting a number of changes called for by ...

This content is provided by an external author without editing by Finextra. It expresses the views and opinions of the author. Traditional device identification has grown increasingly unreliable.

A coalition in late March sent a letter to FDA commissioner Andrew von Eschenbach supporting a mandatory unique device identification (UDI) system and asking him to set a timeline to implement one.

Wireless device identification has evolved from manual feature engineering towards deep learning architectures capable of discerning subtle, hardware-induced differences in transmitted signals. By ...

Forbes contributors publish independent expert analyses and insights. Gary Drenik is a writer covering AI, analytics and innovation. Today’s cybercriminals have countless tools at their disposal to ...

We believe that a CMS requirement to include Unique Device Identifier (UDI) information in billing data is the key to realizing the benefits of a UDI. A Unique Device Identifier (UDI) is an ...

In recent years, the way we interact with our TVs has changed. Multiple button presses to navigate an on-screen keyboard have been replaced with direct interaction through our voices. While this has ...