WALTHAM, Mass.--(BUSINESS WIRE)--Rhinostics, Inc., an innovator in sample collection technologies, today announced that it has received Health Canada approval for sale of its RHINOstic™ Automated ...

Palo Alto, CA -- April 20, 2022 --Mobile authentication pioneer Incognia, today announced the launch of a new location identity fraud detection module to support mobile app security for customers ...

Please provide your email address to receive an email when new articles are posted on . The FDA has granted marketing authorization to Medtronic Inc. for a new device designed to provide continuous ...

SALT LAKE CITY--(BUSINESS WIRE)--Spectrum Solutions, LLC today announced the U.S. Food and Drug Administration (FDA) has extended its Emergency Use Authorization for the SDNA-1000 Saliva Collection ...

We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. Back to Healio The FDA has authorized the marketing of ...

During the COVID-19 public health emergency, the FDA has used its emergency use authorization to allow the use of unapproved medical devices or unapproved uses of authorized medical devices to combat ...

SILVER SPRING, Md., Dec. 21, 2021 /PRNewswire/ -- Today, the U.S. Food and Drug Administration authorized marketing of the first laser-based device for the removal of Inferior Vena Cava (IVC) filters.

During its July 2017 Open Meeting, the Federal Communications Commission (FCC) voted to approve a Report and Order (R&O) containing new rules that impact how RF equipment, manufacturers, vendors, ...