Sensor Patch Market by Product (Blood Glucose Sensor Patch, Blood Oxygen Sensor Patch, Blood Pressure or Flow Sensor Patch), Type (Self-adhesive Sensor Patch, Wearable Sensor Patch), Position, Application, End-User Industry - Global Forecast 2025-2032
Description
The Sensor Patch Market was valued at USD 5.38 billion in 2024 and is projected to grow to USD 6.79 billion in 2025, with a CAGR of 27.85%, reaching USD 38.43 billion by 2032.
A clear and authoritative introduction framing sensor patches as platform-grade biomedical interfaces that bridge real-time physiology and integrated digital health ecosystems
Sensor patch technology is emerging as a pivotal interface between physiology and data, bridging traditional monitoring approaches and continuous, noninvasive health measurement. These thin, often flexible devices integrate biosensing elements, low-power electronics, and adhesive form factors to deliver real-time signals from sweat, interstitial fluid, temperature gradients, and electrical cardiac activity. Early adopters span clinical environments seeking diagnostic augmentation, medical device innovators pursuing therapy-enabled monitoring, and consumer health companies aiming to elevate user engagement through seamless biometrics.
As adoption expands, the conversation has shifted from isolated product demonstrations to systems-level integration. Interoperability expectations, data governance demands, and clinical validation pathways are becoming prerequisites for credible deployment. Consequently, stakeholders must balance rapid product innovation with robust evidentiary frameworks, privacy-preserving data strategies, and manufacturability considerations. This introduction frames sensor patches as platform-grade components within broader digital health architectures, and sets the stage for deeper analysis across regulatory shifts, tariff dynamics, segmentation nuances, regional behaviors, and competitive movements.
Transformative technological, clinical, and regulatory shifts are converging to redefine product priorities and commercialization pathways for next-generation sensor patches
The landscape for sensor patches is undergoing transformative shifts driven by converging advances in materials science, low-power electronics, and data analytics. Flexible substrates and stretchable conductive inks are enabling sensors to conform to complex body contours while maintaining signal fidelity. Concurrently, the maturation of low-power radio and edge processing allows continuous monitoring without prohibitive battery burdens, enabling practical consumer and clinical wearability.
Equally influential are shifts in clinical practice and patient expectations. Telehealth normalization and remote patient monitoring create demand for validated home-friendly devices that can reliably feed longitudinal data into care pathways. Regulatory bodies are adapting evaluation frameworks to accommodate software-enabled diagnostics and hybrid therapy-monitoring combinations, prompting manufacturers to invest earlier in clinical evidence generation and cybersecurity controls. Taken together, these shifts are redefining how stakeholders prioritize product attributes, partnerships, and commercialization strategies-pushing the industry toward modular platforms, evidence-driven design, and integrated service models.
Cumulative tariff-driven supply chain adjustments and sourcing strategies are compelling sensor patch manufacturers to rethink procurement, design, and pricing approaches
Tariff policy changes in the United States have introduced practical complexities for global supply chains supporting sensor patch manufacturing and distribution. Increased import duties on specific electronic components, substrate materials, and finished device classes have prompted component sourcing reviews and supplier diversification efforts. Procurement teams are reassessing supplier contracts to mitigate margin erosion and to preserve predictable lead times for clinical and commercial launches.
In response, manufacturers are evaluating nearshoring and dual-sourcing strategies to reduce exposure to single-origin tariffs while maintaining compliance with regulatory traceability requirements. Design teams are exploring component substitutions and simplifications that retain clinical performance while lowering customs vulnerability. At the same time, contract manufacturers are renegotiating terms to absorb or share tariff impacts, and executives are revising pricing approaches to reflect new landed costs without undermining downstream adoption. These cumulative adjustments are reshaping supplier relationships, inventory policies, and investment plans for capacity expansion.
Key segmentation insights reveal how product modality, device type, positioning, application focus, and end-user industry jointly dictate design, validation, and commercialization priorities
Segmentation insight reveals that product differentiation is increasingly driven by clinical intent and sensing modality, where Blood Glucose Sensor Patch, Blood Oxygen Sensor Patch, Blood Pressure or Flow Sensor Patch, ECG Sensor Patch, Heart Rate Sensor Patch, Pain Reliever, Position Sensor, Sweat Analyzer, and Temperature Sensor Patch each impose distinct validation, materials, and regulatory requirements. Based on Type, the contrast between Self-adhesive Sensor Patch and Wearable Sensor Patch frames different user experience trade-offs: single-application disposability and adhesive biocompatibility versus longer-duration wear and rechargeable electronics. Based on Position, form factor choices such as Bodywear, Footwear, Neckwear, and Wristwear demand divergent mechanical designs, attachment strategies, and signal processing algorithms to account for motion artifacts and contact stability.
Additionally, application focus differentiates development priorities: Diagnostics mandates rigorous clinical endpoints and traceable data lineage, Medical Therapeutics requires tight integration with therapy delivery and fail-safe behavior, and Monitoring emphasizes continuous data streams, low friction, and privacy-respecting analytics. Based on End-User Industry, Fitness & Sports applications prioritize form factor comfort, user engagement, and actionable performance metrics, whereas Healthcare applications emphasize clinical validation, interoperability with electronic health records, and adherence to medical device regulations. These layered segmentation axes inform product roadmaps, go-to-market approaches, and partnership choices, compelling cross-functional teams to align sensing capabilities, user workflows, and regulatory strategies to their targeted segments.
Regional adoption patterns and regulatory diversity are shaping differentiated commercialization strategies across the Americas, Europe, Middle East & Africa, and Asia-Pacific
Regional dynamics shape adoption pathways and partnership opportunities for sensor patch technologies, reflecting variations in regulatory frameworks, reimbursement paradigms, and healthcare delivery models. In the Americas, clinical adoption is driven by integrated care networks and a strong emphasis on remote monitoring initiatives, prompting collaborations between device innovators and health systems to validate real-world utility and care coordination workflows. Europe, Middle East & Africa exhibits a heterogeneous regulatory environment where CE marking pathways and national health technology assessment processes influence market entry sequencing and evidence generation strategies.
The Asia-Pacific region is notable for a dynamic manufacturing ecosystem and rapidly growing consumer health demand, creating fertile ground for scale manufacturing and consumer-oriented wearables. Across regions, local regulatory expectations, clinical trial infrastructure, and payer models determine the optimal commercialization approach. Consequently, cross-border strategies must balance global product standardization with localized evidence packages and reimbursement engagement to accelerate uptake in target jurisdictions.
Competitive and partnership dynamics emphasize integrated hardware, software, and service offerings plus scalable manufacturing as determinants of long-term leadership in sensor patches
Competitive dynamics in the sensor patch arena reflect a blend of specialized startups, diversified medical device companies, and technology incumbents pursuing adjacent opportunities. Companies that pair deep clinical validation with scalable manufacturing tend to secure privileged positions in regulated healthcare settings, while consumer-focused entrants prioritize rapid iteration, strong brand engagement, and app-driven user experiences. Strategic collaborations between materials innovators, semiconductor vendors, and clinical partners are accelerating platform development and reducing time-to-prototype, enabling faster iteration on sensing accuracy and form factor.
Partnership models are evolving from simple supplier relationships to ecosystem plays that bundle device hardware, secure data infrastructure, and analytics services. Contract manufacturers and component suppliers that can offer regulatory-compliant production and transparent supply chain traceability are increasingly influential in selection decisions. Intellectual property around novel sensing chemistries, adhesive systems, and low-noise analog front ends is shaping competitive moats, while service differentiation-such as clinical support, data integration, and outcomes validation-drives enterprise adoption. Observing competitor trajectories suggests that winning strategies will emphasize integrated solutions that meet clinical rigor and scale production reliably.
Actionable priorities for leaders include early clinical validation, resilient sourcing, robust data stewardship, strategic partnerships, and tailored go-to-market approaches
Industry leaders should pursue a pragmatic set of actions to convert technological promise into durable commercial outcomes. First, prioritize evidence generation early in the product lifecycle by aligning clinical validation studies with intended use claims and payor requirements; building such evidence reduces friction in clinical procurement and payer discussions. Second, design for manufacturability and supply chain resilience by qualifying multiple suppliers for critical components and by exploring regional manufacturing options to mitigate tariff and logistics exposure.
Third, commit to data stewardship and interoperability by adopting standardized data models and by implementing robust security and privacy controls that meet regional regulatory expectations. Fourth, cultivate strategic partnerships across materials science, semiconductor providers, and clinical research organizations to accelerate platform maturation while controlling capital intensity. Finally, tailor go-to-market strategies to end-user priorities: emphasize clinical evidence and integration capabilities for healthcare customers, and highlight comfort, usability, and actionable insights for fitness and sports channels. Implementing these actions in sequence will help organizations balance innovation velocity with the operational rigor required for sustained adoption.
A transparent mixed-methods research methodology combining stakeholder interviews, technical literature review, and comparative case study analysis to produce validated strategic insights
The research methodology underpinning this analysis integrated qualitative synthesis and cross-disciplinary validation to ensure balanced, actionable conclusions. Primary inputs included structured interviews with product developers, clinical investigators, procurement leaders, and contract manufacturers, which provided direct insight into design constraints, regulatory expectations, and supply chain practices. Secondary inputs comprised peer-reviewed literature, regulatory guidance documents, and proprietary technical whitepapers that informed assessments of sensing modalities, adhesive biocompatibility, and electronic integration challenges.
Analyses leveraged comparative case studies to identify best practices in evidence generation and manufacturing scale-up. Triangulation techniques were used to reconcile divergent stakeholder perspectives, and expert review sessions validated thematic findings and practical recommendations. Throughout, methodological rigor prioritized transparency of assumptions, reproducibility of analytic steps, and clear delineation between observed practice and forward-looking interpretation, enabling readers to confidently apply these insights to strategic planning and product development efforts.
A clear concluding synthesis emphasizing that cross-functional alignment, evidence generation, and operational excellence are prerequisites for realizing sensor patch potential
In conclusion, sensor patches are positioned to become foundational elements of future care delivery and consumer health engagement, contingent on disciplined attention to evidence, manufacturability, and data integrity. Technological maturation in materials and low-power electronics unlocks compelling form factors, but commercial success will hinge on pairing those innovations with rigorous clinical validation and supply chain resilience. Regulatory clarity and payer engagement remain critical enablers for clinical adoption, while consumer channels will reward comfort, reliability, and seamless data experiences.
Moving forward, organizations that integrate cross-functional expertise-clinical, engineering, regulatory, and commercial-will be best placed to translate prototype promise into scalable solutions. Strategic alignment across these domains reduces commercialization risk and enhances the ability to capture the diverse opportunities that sensor patches present across diagnostics, therapeutics, and monitoring applications. The path to impact is navigable through deliberate investment in evidence, partnerships, and operational excellence.
Note: PDF & Excel + Online Access - 1 Year
A clear and authoritative introduction framing sensor patches as platform-grade biomedical interfaces that bridge real-time physiology and integrated digital health ecosystems
Sensor patch technology is emerging as a pivotal interface between physiology and data, bridging traditional monitoring approaches and continuous, noninvasive health measurement. These thin, often flexible devices integrate biosensing elements, low-power electronics, and adhesive form factors to deliver real-time signals from sweat, interstitial fluid, temperature gradients, and electrical cardiac activity. Early adopters span clinical environments seeking diagnostic augmentation, medical device innovators pursuing therapy-enabled monitoring, and consumer health companies aiming to elevate user engagement through seamless biometrics.
As adoption expands, the conversation has shifted from isolated product demonstrations to systems-level integration. Interoperability expectations, data governance demands, and clinical validation pathways are becoming prerequisites for credible deployment. Consequently, stakeholders must balance rapid product innovation with robust evidentiary frameworks, privacy-preserving data strategies, and manufacturability considerations. This introduction frames sensor patches as platform-grade components within broader digital health architectures, and sets the stage for deeper analysis across regulatory shifts, tariff dynamics, segmentation nuances, regional behaviors, and competitive movements.
Transformative technological, clinical, and regulatory shifts are converging to redefine product priorities and commercialization pathways for next-generation sensor patches
The landscape for sensor patches is undergoing transformative shifts driven by converging advances in materials science, low-power electronics, and data analytics. Flexible substrates and stretchable conductive inks are enabling sensors to conform to complex body contours while maintaining signal fidelity. Concurrently, the maturation of low-power radio and edge processing allows continuous monitoring without prohibitive battery burdens, enabling practical consumer and clinical wearability.
Equally influential are shifts in clinical practice and patient expectations. Telehealth normalization and remote patient monitoring create demand for validated home-friendly devices that can reliably feed longitudinal data into care pathways. Regulatory bodies are adapting evaluation frameworks to accommodate software-enabled diagnostics and hybrid therapy-monitoring combinations, prompting manufacturers to invest earlier in clinical evidence generation and cybersecurity controls. Taken together, these shifts are redefining how stakeholders prioritize product attributes, partnerships, and commercialization strategies-pushing the industry toward modular platforms, evidence-driven design, and integrated service models.
Cumulative tariff-driven supply chain adjustments and sourcing strategies are compelling sensor patch manufacturers to rethink procurement, design, and pricing approaches
Tariff policy changes in the United States have introduced practical complexities for global supply chains supporting sensor patch manufacturing and distribution. Increased import duties on specific electronic components, substrate materials, and finished device classes have prompted component sourcing reviews and supplier diversification efforts. Procurement teams are reassessing supplier contracts to mitigate margin erosion and to preserve predictable lead times for clinical and commercial launches.
In response, manufacturers are evaluating nearshoring and dual-sourcing strategies to reduce exposure to single-origin tariffs while maintaining compliance with regulatory traceability requirements. Design teams are exploring component substitutions and simplifications that retain clinical performance while lowering customs vulnerability. At the same time, contract manufacturers are renegotiating terms to absorb or share tariff impacts, and executives are revising pricing approaches to reflect new landed costs without undermining downstream adoption. These cumulative adjustments are reshaping supplier relationships, inventory policies, and investment plans for capacity expansion.
Key segmentation insights reveal how product modality, device type, positioning, application focus, and end-user industry jointly dictate design, validation, and commercialization priorities
Segmentation insight reveals that product differentiation is increasingly driven by clinical intent and sensing modality, where Blood Glucose Sensor Patch, Blood Oxygen Sensor Patch, Blood Pressure or Flow Sensor Patch, ECG Sensor Patch, Heart Rate Sensor Patch, Pain Reliever, Position Sensor, Sweat Analyzer, and Temperature Sensor Patch each impose distinct validation, materials, and regulatory requirements. Based on Type, the contrast between Self-adhesive Sensor Patch and Wearable Sensor Patch frames different user experience trade-offs: single-application disposability and adhesive biocompatibility versus longer-duration wear and rechargeable electronics. Based on Position, form factor choices such as Bodywear, Footwear, Neckwear, and Wristwear demand divergent mechanical designs, attachment strategies, and signal processing algorithms to account for motion artifacts and contact stability.
Additionally, application focus differentiates development priorities: Diagnostics mandates rigorous clinical endpoints and traceable data lineage, Medical Therapeutics requires tight integration with therapy delivery and fail-safe behavior, and Monitoring emphasizes continuous data streams, low friction, and privacy-respecting analytics. Based on End-User Industry, Fitness & Sports applications prioritize form factor comfort, user engagement, and actionable performance metrics, whereas Healthcare applications emphasize clinical validation, interoperability with electronic health records, and adherence to medical device regulations. These layered segmentation axes inform product roadmaps, go-to-market approaches, and partnership choices, compelling cross-functional teams to align sensing capabilities, user workflows, and regulatory strategies to their targeted segments.
Regional adoption patterns and regulatory diversity are shaping differentiated commercialization strategies across the Americas, Europe, Middle East & Africa, and Asia-Pacific
Regional dynamics shape adoption pathways and partnership opportunities for sensor patch technologies, reflecting variations in regulatory frameworks, reimbursement paradigms, and healthcare delivery models. In the Americas, clinical adoption is driven by integrated care networks and a strong emphasis on remote monitoring initiatives, prompting collaborations between device innovators and health systems to validate real-world utility and care coordination workflows. Europe, Middle East & Africa exhibits a heterogeneous regulatory environment where CE marking pathways and national health technology assessment processes influence market entry sequencing and evidence generation strategies.
The Asia-Pacific region is notable for a dynamic manufacturing ecosystem and rapidly growing consumer health demand, creating fertile ground for scale manufacturing and consumer-oriented wearables. Across regions, local regulatory expectations, clinical trial infrastructure, and payer models determine the optimal commercialization approach. Consequently, cross-border strategies must balance global product standardization with localized evidence packages and reimbursement engagement to accelerate uptake in target jurisdictions.
Competitive and partnership dynamics emphasize integrated hardware, software, and service offerings plus scalable manufacturing as determinants of long-term leadership in sensor patches
Competitive dynamics in the sensor patch arena reflect a blend of specialized startups, diversified medical device companies, and technology incumbents pursuing adjacent opportunities. Companies that pair deep clinical validation with scalable manufacturing tend to secure privileged positions in regulated healthcare settings, while consumer-focused entrants prioritize rapid iteration, strong brand engagement, and app-driven user experiences. Strategic collaborations between materials innovators, semiconductor vendors, and clinical partners are accelerating platform development and reducing time-to-prototype, enabling faster iteration on sensing accuracy and form factor.
Partnership models are evolving from simple supplier relationships to ecosystem plays that bundle device hardware, secure data infrastructure, and analytics services. Contract manufacturers and component suppliers that can offer regulatory-compliant production and transparent supply chain traceability are increasingly influential in selection decisions. Intellectual property around novel sensing chemistries, adhesive systems, and low-noise analog front ends is shaping competitive moats, while service differentiation-such as clinical support, data integration, and outcomes validation-drives enterprise adoption. Observing competitor trajectories suggests that winning strategies will emphasize integrated solutions that meet clinical rigor and scale production reliably.
Actionable priorities for leaders include early clinical validation, resilient sourcing, robust data stewardship, strategic partnerships, and tailored go-to-market approaches
Industry leaders should pursue a pragmatic set of actions to convert technological promise into durable commercial outcomes. First, prioritize evidence generation early in the product lifecycle by aligning clinical validation studies with intended use claims and payor requirements; building such evidence reduces friction in clinical procurement and payer discussions. Second, design for manufacturability and supply chain resilience by qualifying multiple suppliers for critical components and by exploring regional manufacturing options to mitigate tariff and logistics exposure.
Third, commit to data stewardship and interoperability by adopting standardized data models and by implementing robust security and privacy controls that meet regional regulatory expectations. Fourth, cultivate strategic partnerships across materials science, semiconductor providers, and clinical research organizations to accelerate platform maturation while controlling capital intensity. Finally, tailor go-to-market strategies to end-user priorities: emphasize clinical evidence and integration capabilities for healthcare customers, and highlight comfort, usability, and actionable insights for fitness and sports channels. Implementing these actions in sequence will help organizations balance innovation velocity with the operational rigor required for sustained adoption.
A transparent mixed-methods research methodology combining stakeholder interviews, technical literature review, and comparative case study analysis to produce validated strategic insights
The research methodology underpinning this analysis integrated qualitative synthesis and cross-disciplinary validation to ensure balanced, actionable conclusions. Primary inputs included structured interviews with product developers, clinical investigators, procurement leaders, and contract manufacturers, which provided direct insight into design constraints, regulatory expectations, and supply chain practices. Secondary inputs comprised peer-reviewed literature, regulatory guidance documents, and proprietary technical whitepapers that informed assessments of sensing modalities, adhesive biocompatibility, and electronic integration challenges.
Analyses leveraged comparative case studies to identify best practices in evidence generation and manufacturing scale-up. Triangulation techniques were used to reconcile divergent stakeholder perspectives, and expert review sessions validated thematic findings and practical recommendations. Throughout, methodological rigor prioritized transparency of assumptions, reproducibility of analytic steps, and clear delineation between observed practice and forward-looking interpretation, enabling readers to confidently apply these insights to strategic planning and product development efforts.
A clear concluding synthesis emphasizing that cross-functional alignment, evidence generation, and operational excellence are prerequisites for realizing sensor patch potential
In conclusion, sensor patches are positioned to become foundational elements of future care delivery and consumer health engagement, contingent on disciplined attention to evidence, manufacturability, and data integrity. Technological maturation in materials and low-power electronics unlocks compelling form factors, but commercial success will hinge on pairing those innovations with rigorous clinical validation and supply chain resilience. Regulatory clarity and payer engagement remain critical enablers for clinical adoption, while consumer channels will reward comfort, reliability, and seamless data experiences.
Moving forward, organizations that integrate cross-functional expertise-clinical, engineering, regulatory, and commercial-will be best placed to translate prototype promise into scalable solutions. Strategic alignment across these domains reduces commercialization risk and enhances the ability to capture the diverse opportunities that sensor patches present across diagnostics, therapeutics, and monitoring applications. The path to impact is navigable through deliberate investment in evidence, partnerships, and operational excellence.
Note: PDF & Excel + Online Access - 1 Year
Table of Contents
196 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. Advances in flexible biocompatible materials extending continuous wear time of sensor patches
- 5.2. Integration of AI-driven predictive analytics for remote patient monitoring via sensor patches
- 5.3. Regulatory approvals and reimbursement pathways accelerating noninvasive glucose sensor patch adoption
- 5.4. Collaboration between pharma and device manufacturers to develop targeted drug delivery sensor patches
- 5.5. Emergence of wireless power transfer technologies to extend battery life of continuous monitoring patches
- 5.6. Growth of multi-analyte wearable sensor patches providing real-time biomarker tracking through smartphones
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Sensor Patch Market, by Product
- 8.1. Blood Glucose Sensor Patch
- 8.2. Blood Oxygen Sensor Patch
- 8.3. Blood Pressure or Flow Sensor Patch
- 8.4. ECG Sensor Patch
- 8.5. Heart Rate Sensor Patch
- 8.6. Pain Reliever
- 8.7. Position Sensor
- 8.8. Sweat Analyzer
- 8.9. Temperature Sensor Patch
- 9. Sensor Patch Market, by Type
- 9.1. Self-adhesive Sensor Patch
- 9.2. Wearable Sensor Patch
- 10. Sensor Patch Market, by Position
- 10.1. Bodywear
- 10.2. Footwear
- 10.3. Neckwear
- 10.4. Wristwear
- 11. Sensor Patch Market, by Application
- 11.1. Diagnostics
- 11.2. Medical Therapeutics
- 11.3. Monitoring
- 12. Sensor Patch Market, by End-User Industry
- 12.1. Fitness & Sports
- 12.2. Healthcare
- 13. Sensor Patch 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. Sensor Patch Market, by Group
- 14.1. ASEAN
- 14.2. GCC
- 14.3. European Union
- 14.4. BRICS
- 14.5. G7
- 14.6. NATO
- 15. Sensor Patch 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. Abbott Laboratories
- 16.3.2. accensors GmbH
- 16.3.3. Beneli AB
- 16.3.4. Blue Spark Technologies, Inc.
- 16.3.5. Boston Scientific Corporation
- 16.3.6. Boyd Corporation
- 16.3.7. Covestro AG
- 16.3.8. Dexcom, Inc.
- 16.3.9. DuPont de Nemours, Inc.
- 16.3.10. G-Tech Medical Inc.
- 16.3.11. GE HealthCare Technologies, Inc.
- 16.3.12. Gentag, Inc.
- 16.3.13. GTECH Corporation
- 16.3.14. iRhythm Technologies, Inc.
- 16.3.15. Isansys Lifecare Ltd.
- 16.3.16. Kenzen, Inc.
- 16.3.17. Koninklijke Philips N.V.
- 16.3.18. LifeSignals, Inc. by Renew Health Limited
- 16.3.19. Masimo Corporation
- 16.3.20. Medtronic PLC
- 16.3.21. NanoSonic, Inc.
- 16.3.22. Nemaura Medical Inc.
- 16.3.23. Nitto Denko Corporation
- 16.3.24. PolarSeal Tapes & Conversions Ltd.
- 16.3.25. Resonetics
- 16.3.26. Sensium Healthcare Limited by The Surgical Company group
- 16.3.27. Smith+Nephew PLC
- 16.3.28. VitalConnect
- 16.3.29. VivaLNK, Inc.
- 16.3.30. Vpatch Cardio Pty Ltd.
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