Press Center
Stay Informed with the Latest KORE News, Insights, and Industry Updates
news
KORE Appoints Jared Deith as Chief Revenue Officer to Accelerate Market Leadership and Innovation
ATLANTA – January 31, 2025 – KORE Group Holdings, Inc. (NYSE: KORE) (“KORE” or the “Company”), a global leader in IoT solutions and pioneering IoT hyperscaler, and provider of IoT Connectivity,…
KORE Receives 2024 IoT Excellence Award
KORE Super SIM® Honored for Excellence in Innovation ATLANTA – (January 24, 2025) – KORE, a global leader in Internet of Things (“IoT”) Solutions and provider of IoT Connectivity, Solutions and…
Sensors in Agriculture: What Are They All About?
Agriculture comes with many challenges. There are labor shortages, climate unpredictability, poor soil from lacking land management, and more. These challenges can make agriculture difficult, but technology has provided a…
press mentions
The State of IoT: Transformative Momentum and What Lies Ahead
KORE in-vehicle video solution recognised with award
The Backbone of Virtual Healthcare: Ensuring Seamless Connectivity Anywhere
Positioned as Leaders for 5th time in a row
awards
IoT Breakthrough Awards – 2025
Connected Car Product of the Year – KORE In-Vehicle Video
IDC Marketscape – 2023
Positioned as Leader in Worldwide Managed IoT Connectivity Services 2023 Vendor Assessment
certifications
ISO 9001 Certified
Demonstrates compliance with internationally recognized quality management system standards, ensuring consistent product and service quality.
ISO 13485 Certifiedt
Specifies requirements for a quality management system in the design, production, and distribution of medical devices, ensuring regulatory compliance and patient safety.
FDA Registration 21 CFR Part 820 Compliant
Indicates adherence to the FDA’s Quality System Regulation (QSR) for medical device manufacturing, ensuring products meet safety and efficacy requirements.
Medical Device Re-Packaging Facility, Contract Manufacturer, Re-packager/Re-labeler
Certifies authorisation to manufacture, repackage, and relabel medical devices in compliance with regulatory standards.
2015 EU/EEA/CH Country Specific Registration
Ensures compliance with country-specific medical device regulations across the EU, European Economic Area (EEA), and Switzerland.
2015 EU MDD 9X/XX/EC Compliance
Confirms conformity with the European Union’s Medical Devices Directive (MDD), allowing legal market access in the EU.