Insulin Storage Devices Market by Product Type (Active Storage Devices, Passive Storage Devices, Smart Storage Systems), Mode Of Operation (Active, Passive), Technology, End User, Distribution Channel - Global Forecast 2025-2032
Description
The Insulin Storage Devices Market was valued at USD 1.02 billion in 2024 and is projected to grow to USD 1.09 billion in 2025, with a CAGR of 8.23%, reaching USD 1.92 billion by 2032.
Framing the evolving priorities of device reliability, patient-centric cold-chain management, and regulatory alignment across clinical and home settings
The insulin storage devices landscape sits at the intersection of clinical safety, patient empowerment, and logistical complexity. Growing prevalence of insulin-dependent conditions has elevated the importance of reliable cold-chain solutions across home, clinical, and retail environments. As devices evolve from passive coolers to connected systems, stakeholders must reconcile regulatory rigor with real-world use conditions, ensuring that design, testing, and distribution practices prevent temperature excursions that can compromise therapeutic efficacy.
In response, manufacturers, healthcare providers, and distributors are refining product attributes and service models to prioritize consistent temperature maintenance, ease of use, and traceable monitoring. This report frames key drivers shaping product development, highlights operational pain points in last-mile handling, and identifies the technical and organizational levers that influence adoption decisions. By situating device performance within patient journeys and care pathways, the introduction emphasizes pragmatic strategies that align safety objectives with scalable commercial models.
How technological convergence, regulatory focus on traceability, and collaborative supply-chain models are reshaping insulin storage device priorities and adoption
The insulin storage device sector is experiencing transformative shifts driven by converging forces in technology, regulation, and user expectations. Advances in low-power electronics and thermoelectric materials are enabling smaller active cooling units that bridge the gap between portable convenience and clinical-grade temperature stability. Meanwhile, IoT-enabled monitoring and mobile integration are redefining product value by enabling real-time alerts, audit trails, and predictive maintenance capabilities that were previously limited to institutional settings.
Concurrently, regulatory emphasis on supply chain traceability and post-market surveillance is prompting manufacturers to embed more robust monitoring features and standardized validation protocols. As a result, companies that invest in interoperable platforms and rigorous compliance pathways are better positioned to build trust among clinicians and caregivers. Transitionary initiatives, such as partnerships between device makers and logistics providers, illustrate how ecosystem collaboration can reduce last-mile failures and broaden access, particularly for patients who require travel or refrigeration alternatives outside conventional clinical environments.
Implications of 2025 tariff adjustments on sourcing strategies, landed costs, and supply-chain resilience for insulin storage device manufacturers and buyers
Tariff policy shifts enacted in 2025 have introduced new considerations for manufacturers and supply-chain planners operating within and across U.S. borders. Increased duties on select imported components and finished devices have elevated landed-cost sensitivity, encouraging firms to reassess sourcing footprints, supplier relationships, and inventory strategies. In response, several manufacturers are evaluating nearshoring options or expanding domestic assembly capabilities to preserve margin and control lead times.
These changes have also prompted procurement and regulatory teams to revisit supplier qualification criteria, emphasizing resilience and local compliance expertise. As trade policy influences component selection, design teams face trade-offs between cost, performance, and maintainability. For distributors and healthcare providers, the immediate effect has been a renewed focus on total-cost-of-ownership evaluations that incorporate tariff exposure, logistics volatility, and service-level implications. Over time, strategic decisions taken in reaction to tariff shifts could accelerate localization of critical subassemblies and incentivize design simplification to reduce reliance on tariff-impacted imports.
In-depth segmentation analysis revealing product architectures, operational modes, technological pathways, end-user demands, and distribution channels that drive competitive differentiation
Product segmentation reveals distinct development and use-case patterns that are shaping competitive positioning and procurement logic. Based on product type, the market encompasses Active Storage Devices, Passive Storage Devices, Smart Storage Systems, and Temperature Monitoring Devices; Active Storage Devices further divide into battery-powered coolers and electric refrigerated units while Passive Storage Devices extend into cooler boxes, foam containers, and insulated bags, Smart Storage Systems include Bluetooth temperature monitors and IoT-enabled refrigerators, and Temperature Monitoring Devices separate into integrated monitoring solutions and standalone data loggers. Each product tier balances trade-offs between portability, thermal stability, usability, and cost, with active solutions appealing where sustained cooling is required and passive options remaining central to low-cost, last-mile distribution.
When viewed through the mode of operation lens, the market is characterized by Active and Passive approaches; Active modes include electric cooling and thermoelectric cooling while Passive approaches rely on dry ice, gel packs, and phase change materials. This distinction drives different validation, charging, and handling procedures, and informs regulatory and end-user training requirements. Technological segmentation highlights choices among electric cooling technology, gel pack systems, IoT-enabled monitoring, and phase change materials; electric cooling technology itself subdivides into compressor cooling and thermoelectric solutions while IoT-enabled monitoring further differentiates into cloud-enabled platforms and mobile app integration. These technology splits influence integration complexity, power requirements, and data capabilities that are critical for clinical adoption.
End-user segmentation underscores divergent needs among home users, hospitals and clinics, pharmacies, and research laboratories; hospitals and clinics further separate into private clinics and public hospitals while pharmacies differentiate between hospital pharmacies and retail pharmacies. Finally, distribution channel segmentation reflects offline and online pathways; offline channels comprise hospital channels, medical device distributors, and pharmacy channels while online channels include ecommerce platforms and manufacturer websites. Understanding how these segments intersect helps stakeholders tailor product feature sets, service models, and go-to-market strategies to meet specific operational constraints and user expectations.
Regional dynamics shaping product design, regulatory navigation, and go-to-market approaches across the Americas, Europe Middle East & Africa, and Asia-Pacific environments
Regional dynamics are exerting powerful influence on product design choices, regulatory compliance priorities, and commercialization tactics. In the Americas, mature healthcare infrastructure and high prevalence of home-based insulin use emphasize portability, connectivity, and integration with patient support services, encouraging vendors to prioritize user-friendly interfaces and post-sale service networks. In contrast, Europe, Middle East & Africa presents a heterogeneous regulatory and delivery environment; Western European markets demand stringent compliance and interoperability, while emerging markets across the Middle East and Africa prioritize ruggedness, low-cost passive solutions, and supply-chain robustness to manage distribution in challenging climates.
Across Asia-Pacific, rapid technology adoption, strong manufacturing capacity, and diverse end-user settings create both high-volume opportunities and complex localization requirements. Regional preferences influence everything from battery specifications to documentation and language support, and transitional dynamics between these regions drive cross-border partnerships and localized manufacturing strategies. Consequently, companies that map regional clinical practices and distribution realities into modular product architectures gain advantages in both regulatory navigation and customer acceptance.
Competitive landscapes and capability clusters defined by thermal performance, digital integration, regulatory expertise, and strategic channel partnerships
Competitive positioning in insulin storage devices is anchored in a combination of thermal performance, connectivity, regulatory compliance, and channel reach. Established medical device manufacturers leverage deep regulatory experience and broad distribution networks to serve institutional buyers, while agile startups differentiate through integrated digital features, novel phase change materials, or lightweight active cooling systems optimized for home use. Strategic partnerships between device makers and logistics or software providers are becoming more common, enabling bundled offerings that combine hardware reliability with data services for monitoring, maintenance, and compliance documentation.
Intellectual property around thermoelectric materials, battery-efficient control algorithms, and secure data transmission is increasingly important, shaping both product roadmaps and M&A discussions. Companies that can demonstrate validated performance across a range of environmental conditions and that offer clear pathways for integration with clinical record systems earn higher credibility among hospital procurement teams. At the same time, strong aftermarket support, warranty programs, and accessible service networks influence adoption among pharmacies and home users, where product downtime or user confusion can directly impact therapeutic continuity.
Actionable strategic priorities for manufacturers and stakeholders to enhance product resilience, regulatory readiness, and integrated cold-chain services
Industry leaders should prioritize integrated reliability and user experience while aligning supply-chain architecture with evolving trade and regulatory risks. First, invest in modular product platforms that allow rapid configuration between active and passive variants and that accommodate regional power and labeling requirements. Second, accelerate integration of secure, low-power monitoring that provides auditable temperature records and mobile alerts, thereby increasing clinical trust and enabling value-added services.
Additionally, reassess supplier footprints to reduce exposure to tariff volatility and long lead times by identifying viable nearshoring or dual-sourcing options for critical subcomponents. Strengthen post-sale support by deploying standardized training materials and streamlined warranty processes that reduce service friction for clinicians and caregivers. Finally, cultivate partnerships with logistics and healthcare IT providers to deliver bundled cold-chain solutions, aligning device performance with handling protocols and digital recordkeeping to minimize temperature excursions and enhance patient safety.
Methodological overview combining expert interviews, hands-on device evaluation, regulatory analysis, and scenario-based supply-chain risk assessment to validate findings
This research synthesizes qualitative expert interviews, technical device assessments, and cross-functional analysis of supply-chain and regulatory frameworks to deliver actionable insights. Primary inputs included structured discussions with device engineers, clinical pharmacists, and logistics leaders, combined with hands-on evaluation of representative products to assess thermal behavior, power consumption, and user interfaces under real-world conditions. Secondary inputs encompassed regulatory guidance documents, standards for temperature-sensitive therapeutics, and publicly available case studies that illustrate deployment challenges in varied care settings.
Analytical methods integrated comparative device profiling, scenario-based risk assessment for supply-chain disruptions, and technology readiness evaluations that consider integration complexity and post-market support requirements. Throughout the process, findings were validated through iterative consultations with subject-matter experts to ensure practical relevance and to align conclusions with operational realities faced by manufacturers, distributors, and care providers.
Synthesis of how engineering, connectivity, and supply-chain strategy converge to advance safe and scalable insulin storage solutions across care settings
In conclusion, insulin storage devices are undergoing a period of pragmatic innovation where thermal science, connectivity, and supply-chain strategy converge to shape practical solutions for patients and providers. The evolution from simple passive containers toward hybrid systems and connected monitoring reflects an industry response to demands for reliable temperature management, traceability, and ease of use across home and institutional environments. While trade policy shifts and regional nuances add complexity, they also catalyze strategic choices that enhance resilience and market alignment.
Looking ahead, organizations that combine robust engineering, clear regulatory pathways, and integrated service models will be best positioned to reduce cold-chain failures and improve therapeutic outcomes. By focusing on modular designs, validated monitoring, and pragmatic channel strategies, stakeholders can deliver solutions that meet clinical requirements while remaining adaptable to changing logistical and policy environments.
Please Note: PDF & Excel + Online Access - 1 Year
Framing the evolving priorities of device reliability, patient-centric cold-chain management, and regulatory alignment across clinical and home settings
The insulin storage devices landscape sits at the intersection of clinical safety, patient empowerment, and logistical complexity. Growing prevalence of insulin-dependent conditions has elevated the importance of reliable cold-chain solutions across home, clinical, and retail environments. As devices evolve from passive coolers to connected systems, stakeholders must reconcile regulatory rigor with real-world use conditions, ensuring that design, testing, and distribution practices prevent temperature excursions that can compromise therapeutic efficacy.
In response, manufacturers, healthcare providers, and distributors are refining product attributes and service models to prioritize consistent temperature maintenance, ease of use, and traceable monitoring. This report frames key drivers shaping product development, highlights operational pain points in last-mile handling, and identifies the technical and organizational levers that influence adoption decisions. By situating device performance within patient journeys and care pathways, the introduction emphasizes pragmatic strategies that align safety objectives with scalable commercial models.
How technological convergence, regulatory focus on traceability, and collaborative supply-chain models are reshaping insulin storage device priorities and adoption
The insulin storage device sector is experiencing transformative shifts driven by converging forces in technology, regulation, and user expectations. Advances in low-power electronics and thermoelectric materials are enabling smaller active cooling units that bridge the gap between portable convenience and clinical-grade temperature stability. Meanwhile, IoT-enabled monitoring and mobile integration are redefining product value by enabling real-time alerts, audit trails, and predictive maintenance capabilities that were previously limited to institutional settings.
Concurrently, regulatory emphasis on supply chain traceability and post-market surveillance is prompting manufacturers to embed more robust monitoring features and standardized validation protocols. As a result, companies that invest in interoperable platforms and rigorous compliance pathways are better positioned to build trust among clinicians and caregivers. Transitionary initiatives, such as partnerships between device makers and logistics providers, illustrate how ecosystem collaboration can reduce last-mile failures and broaden access, particularly for patients who require travel or refrigeration alternatives outside conventional clinical environments.
Implications of 2025 tariff adjustments on sourcing strategies, landed costs, and supply-chain resilience for insulin storage device manufacturers and buyers
Tariff policy shifts enacted in 2025 have introduced new considerations for manufacturers and supply-chain planners operating within and across U.S. borders. Increased duties on select imported components and finished devices have elevated landed-cost sensitivity, encouraging firms to reassess sourcing footprints, supplier relationships, and inventory strategies. In response, several manufacturers are evaluating nearshoring options or expanding domestic assembly capabilities to preserve margin and control lead times.
These changes have also prompted procurement and regulatory teams to revisit supplier qualification criteria, emphasizing resilience and local compliance expertise. As trade policy influences component selection, design teams face trade-offs between cost, performance, and maintainability. For distributors and healthcare providers, the immediate effect has been a renewed focus on total-cost-of-ownership evaluations that incorporate tariff exposure, logistics volatility, and service-level implications. Over time, strategic decisions taken in reaction to tariff shifts could accelerate localization of critical subassemblies and incentivize design simplification to reduce reliance on tariff-impacted imports.
In-depth segmentation analysis revealing product architectures, operational modes, technological pathways, end-user demands, and distribution channels that drive competitive differentiation
Product segmentation reveals distinct development and use-case patterns that are shaping competitive positioning and procurement logic. Based on product type, the market encompasses Active Storage Devices, Passive Storage Devices, Smart Storage Systems, and Temperature Monitoring Devices; Active Storage Devices further divide into battery-powered coolers and electric refrigerated units while Passive Storage Devices extend into cooler boxes, foam containers, and insulated bags, Smart Storage Systems include Bluetooth temperature monitors and IoT-enabled refrigerators, and Temperature Monitoring Devices separate into integrated monitoring solutions and standalone data loggers. Each product tier balances trade-offs between portability, thermal stability, usability, and cost, with active solutions appealing where sustained cooling is required and passive options remaining central to low-cost, last-mile distribution.
When viewed through the mode of operation lens, the market is characterized by Active and Passive approaches; Active modes include electric cooling and thermoelectric cooling while Passive approaches rely on dry ice, gel packs, and phase change materials. This distinction drives different validation, charging, and handling procedures, and informs regulatory and end-user training requirements. Technological segmentation highlights choices among electric cooling technology, gel pack systems, IoT-enabled monitoring, and phase change materials; electric cooling technology itself subdivides into compressor cooling and thermoelectric solutions while IoT-enabled monitoring further differentiates into cloud-enabled platforms and mobile app integration. These technology splits influence integration complexity, power requirements, and data capabilities that are critical for clinical adoption.
End-user segmentation underscores divergent needs among home users, hospitals and clinics, pharmacies, and research laboratories; hospitals and clinics further separate into private clinics and public hospitals while pharmacies differentiate between hospital pharmacies and retail pharmacies. Finally, distribution channel segmentation reflects offline and online pathways; offline channels comprise hospital channels, medical device distributors, and pharmacy channels while online channels include ecommerce platforms and manufacturer websites. Understanding how these segments intersect helps stakeholders tailor product feature sets, service models, and go-to-market strategies to meet specific operational constraints and user expectations.
Regional dynamics shaping product design, regulatory navigation, and go-to-market approaches across the Americas, Europe Middle East & Africa, and Asia-Pacific environments
Regional dynamics are exerting powerful influence on product design choices, regulatory compliance priorities, and commercialization tactics. In the Americas, mature healthcare infrastructure and high prevalence of home-based insulin use emphasize portability, connectivity, and integration with patient support services, encouraging vendors to prioritize user-friendly interfaces and post-sale service networks. In contrast, Europe, Middle East & Africa presents a heterogeneous regulatory and delivery environment; Western European markets demand stringent compliance and interoperability, while emerging markets across the Middle East and Africa prioritize ruggedness, low-cost passive solutions, and supply-chain robustness to manage distribution in challenging climates.
Across Asia-Pacific, rapid technology adoption, strong manufacturing capacity, and diverse end-user settings create both high-volume opportunities and complex localization requirements. Regional preferences influence everything from battery specifications to documentation and language support, and transitional dynamics between these regions drive cross-border partnerships and localized manufacturing strategies. Consequently, companies that map regional clinical practices and distribution realities into modular product architectures gain advantages in both regulatory navigation and customer acceptance.
Competitive landscapes and capability clusters defined by thermal performance, digital integration, regulatory expertise, and strategic channel partnerships
Competitive positioning in insulin storage devices is anchored in a combination of thermal performance, connectivity, regulatory compliance, and channel reach. Established medical device manufacturers leverage deep regulatory experience and broad distribution networks to serve institutional buyers, while agile startups differentiate through integrated digital features, novel phase change materials, or lightweight active cooling systems optimized for home use. Strategic partnerships between device makers and logistics or software providers are becoming more common, enabling bundled offerings that combine hardware reliability with data services for monitoring, maintenance, and compliance documentation.
Intellectual property around thermoelectric materials, battery-efficient control algorithms, and secure data transmission is increasingly important, shaping both product roadmaps and M&A discussions. Companies that can demonstrate validated performance across a range of environmental conditions and that offer clear pathways for integration with clinical record systems earn higher credibility among hospital procurement teams. At the same time, strong aftermarket support, warranty programs, and accessible service networks influence adoption among pharmacies and home users, where product downtime or user confusion can directly impact therapeutic continuity.
Actionable strategic priorities for manufacturers and stakeholders to enhance product resilience, regulatory readiness, and integrated cold-chain services
Industry leaders should prioritize integrated reliability and user experience while aligning supply-chain architecture with evolving trade and regulatory risks. First, invest in modular product platforms that allow rapid configuration between active and passive variants and that accommodate regional power and labeling requirements. Second, accelerate integration of secure, low-power monitoring that provides auditable temperature records and mobile alerts, thereby increasing clinical trust and enabling value-added services.
Additionally, reassess supplier footprints to reduce exposure to tariff volatility and long lead times by identifying viable nearshoring or dual-sourcing options for critical subcomponents. Strengthen post-sale support by deploying standardized training materials and streamlined warranty processes that reduce service friction for clinicians and caregivers. Finally, cultivate partnerships with logistics and healthcare IT providers to deliver bundled cold-chain solutions, aligning device performance with handling protocols and digital recordkeeping to minimize temperature excursions and enhance patient safety.
Methodological overview combining expert interviews, hands-on device evaluation, regulatory analysis, and scenario-based supply-chain risk assessment to validate findings
This research synthesizes qualitative expert interviews, technical device assessments, and cross-functional analysis of supply-chain and regulatory frameworks to deliver actionable insights. Primary inputs included structured discussions with device engineers, clinical pharmacists, and logistics leaders, combined with hands-on evaluation of representative products to assess thermal behavior, power consumption, and user interfaces under real-world conditions. Secondary inputs encompassed regulatory guidance documents, standards for temperature-sensitive therapeutics, and publicly available case studies that illustrate deployment challenges in varied care settings.
Analytical methods integrated comparative device profiling, scenario-based risk assessment for supply-chain disruptions, and technology readiness evaluations that consider integration complexity and post-market support requirements. Throughout the process, findings were validated through iterative consultations with subject-matter experts to ensure practical relevance and to align conclusions with operational realities faced by manufacturers, distributors, and care providers.
Synthesis of how engineering, connectivity, and supply-chain strategy converge to advance safe and scalable insulin storage solutions across care settings
In conclusion, insulin storage devices are undergoing a period of pragmatic innovation where thermal science, connectivity, and supply-chain strategy converge to shape practical solutions for patients and providers. The evolution from simple passive containers toward hybrid systems and connected monitoring reflects an industry response to demands for reliable temperature management, traceability, and ease of use across home and institutional environments. While trade policy shifts and regional nuances add complexity, they also catalyze strategic choices that enhance resilience and market alignment.
Looking ahead, organizations that combine robust engineering, clear regulatory pathways, and integrated service models will be best positioned to reduce cold-chain failures and improve therapeutic outcomes. By focusing on modular designs, validated monitoring, and pragmatic channel strategies, stakeholders can deliver solutions that meet clinical requirements while remaining adaptable to changing logistical and policy environments.
Please Note: PDF & Excel + Online Access - 1 Year
Table of Contents
181 Pages
- 1. Preface
- 1.1. Objectives of the Study
- 1.2. Market Segmentation & Coverage
- 1.3. Years Considered for the Study
- 1.4. Currency
- 1.5. Language
- 1.6. Stakeholders
- 2. Research Methodology
- 3. Executive Summary
- 4. Market Overview
- 5. Market Insights
- 5.1. Development of temperature-controlled smart insulin pens with integrated connectivity for real-time dosage monitoring
- 5.2. Adoption of phase-change material-based portable insulin shipping containers for extended cold chain maintenance
- 5.3. Integration of wireless temperature sensors in home insulin refrigerators for proactive spoilage prevention alerts
- 5.4. Use of solar-powered active cooling units for insulin storage in remote and off-grid healthcare settings
- 5.5. Collaboration between pharmaceutical manufacturers and IoT firms to standardize Bluetooth-enabled insulin vial trackers
- 5.6. Surging demand for phase-change insulated travel pouches with smartphone-linked temperature monitoring among diabetic patients
- 5.7. Regulatory emphasis on validated thermal performance data for consumer-grade insulin cooling devices
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Insulin Storage Devices Market, by Product Type
- 8.1. Active Storage Devices
- 8.1.1. Battery-Powered Coolers
- 8.1.2. Electric Refrigerated Units
- 8.2. Passive Storage Devices
- 8.2.1. Cooler Boxes
- 8.2.2. Foam Containers
- 8.2.3. Insulated Bags
- 8.3. Smart Storage Systems
- 8.3.1. Bluetooth Temperature Monitors
- 8.3.2. IoT Enabled Refrigerators
- 8.4. Temperature Monitoring Devices
- 8.4.1. Integrated Monitoring Solutions
- 8.4.2. Standalone Data Loggers
- 9. Insulin Storage Devices Market, by Mode Of Operation
- 9.1. Active
- 9.1.1. Electric Cooling
- 9.1.2. Thermoelectric Cooling
- 9.2. Passive
- 9.2.1. Dry Ice
- 9.2.2. Gel Pack Based
- 9.2.3. Phase Change Materials
- 10. Insulin Storage Devices Market, by Technology
- 10.1. Electric Cooling Technology
- 10.1.1. Compressor Cooling
- 10.1.2. Thermoelectric Solutions
- 10.2. Gel Pack
- 10.3. IoT Enabled Monitoring
- 10.3.1. Cloud Enabled Platforms
- 10.3.2. Mobile App Integration
- 10.4. Phase Change Material
- 11. Insulin Storage Devices Market, by End User
- 11.1. Home Users
- 11.2. Hospitals & Clinics
- 11.2.1. Private Clinics
- 11.2.2. Public Hospitals
- 11.3. Pharmacies
- 11.3.1. Hospital Pharmacies
- 11.3.2. Retail Pharmacies
- 11.4. Research Laboratories
- 12. Insulin Storage Devices Market, by Distribution Channel
- 12.1. Offline
- 12.1.1. Hospital Channels
- 12.1.2. Medical Device Distributors
- 12.1.3. Pharmacy Channels
- 12.2. Online
- 12.2.1. ECommerce Platforms
- 12.2.2. Manufacturer Websites
- 13. Insulin Storage Devices Market, by Region
- 13.1. Americas
- 13.1.1. North America
- 13.1.2. Latin America
- 13.2. Europe, Middle East & Africa
- 13.2.1. Europe
- 13.2.2. Middle East
- 13.2.3. Africa
- 13.3. Asia-Pacific
- 14. Insulin Storage Devices Market, by Group
- 14.1. ASEAN
- 14.2. GCC
- 14.3. European Union
- 14.4. BRICS
- 14.5. G7
- 14.6. NATO
- 15. Insulin Storage Devices Market, by Country
- 15.1. United States
- 15.2. Canada
- 15.3. Mexico
- 15.4. Brazil
- 15.5. United Kingdom
- 15.6. Germany
- 15.7. France
- 15.8. Russia
- 15.9. Italy
- 15.10. Spain
- 15.11. China
- 15.12. India
- 15.13. Japan
- 15.14. Australia
- 15.15. South Korea
- 16. Competitive Landscape
- 16.1. Market Share Analysis, 2024
- 16.2. FPNV Positioning Matrix, 2024
- 16.3. Competitive Analysis
- 16.3.1. Medtronic plc
- 16.3.2. Insulet Corporation
- 16.3.3. Tandem Diabetes Care Inc.
- 16.3.4. Novo Nordisk A/S
- 16.3.5. Eli Lilly and Company
- 16.3.6. Sanofi S.A.
- 16.3.7. Roche Diabetes Care Inc.
- 16.3.8. Abbott Laboratories
- 16.3.9. Ypsomed Holding AG
- 16.3.10. Companion Medical Inc.
- 16.3.11. Emperra GmbH E-Health Technologies
- 16.3.12. Diabeloop SA
- 16.3.13. Jiangsu Delfu Medical Device Co. Ltd.
- 16.3.14. GlucoRx Limited
- 16.3.15. Mikro Systems Inc.
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