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news
KORE Reschedules Earnings Release and Conference Call
ATLANTA (April 15, 2025) – KORE Group Holdings, Inc. (NYSE: KORE) (“KORE” or the “Company”)), a global leader in Internet of Things (“IoT”) solutions and pioneering IoT hyperscaler, today announced…
KORE to Report Fourth Quarter and Full Year 2024 Results on April 15, 2025
ATLANTA – March 31, 2025 – KORE Group Holdings, Inc. (NYSE: KORE) (“KORE” or the “Company”), the global pure-play Internet of Things (“IoT”) hyperscaler, and provider of IoT Connectivity, Solutions…
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,…
press mentions
The Edge Evolution: New Frontiers in IoT and Cellular Computing
The State of IoT: Transformative Momentum and What Lies Ahead
KORE in-vehicle video solution recognised with award
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.