Press Center
Stay Informed with the Latest KORE News, Insights, and Industry Updates
news
KORE Announces Chief Financial Officer Transition
Anthony Bellomo Appointed Executive Vice President and Chief Financial Officer ATLANTA (June 2, 2025) – KORE Group Holdings, Inc. (“KORE” or the “Company”), a global leader in Internet of Things…
KORE Reports First Quarter 2025 Results
Growth in Connections, Operating Cash and Free Cash Flow ATLANTA – May 15, 2025 – KORE Group Holdings, Inc. (NYSE: KORE) (“KORE” or the “Company”), the global pure-play Internet of…
KORE, Robo, Ericsson, and Winnebago Redefine the Open Road with Winnebago Connect™
A Seamless, Smarter RV Experience Powered by IoT Innovation ATLANTA (May 12, 2025) – KORE, a global leader in Internet of Things (“IoT”) Solutions and IoT Connectivity provider, has collaborated…
press mentions
KORE, Robo, Ericsson, and Winnebago Redefine the Open Road with Winnebago Connect™
Bevi Unveils The Countertop 1.5: A Smaller and Mightier Smart Water Dispenser
From IoT to the Innovation of Things: A Conversation with Jared Deith, EVP & CRO at KORE
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 Certified
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.