Dental Adhesives & Sealants Market by Product Type (Adhesives, Sealants), Material Type (Glass Ionomer Based, Hybrid, Resin Based), End User, Distribution Channel, Application - Global Forecast 2025-2032
Description
The Dental Adhesives & Sealants Market was valued at USD 4.83 billion in 2024 and is projected to grow to USD 5.17 billion in 2025, with a CAGR of 7.16%, reaching USD 8.40 billion by 2032.
Introduction framing clinical needs, material science advances, regulatory evolution, and commercial dynamics shaping modern dental adhesives and sealants
The dental adhesives and sealants domain sits at the intersection of clinical demands, material science advances, and evolving regulatory frameworks, making it an essential focus for clinicians, manufacturers, and procurement leaders. Clinicians continue to demand materials that deliver reliable bonding, ease of use, and long-term clinical performance, while manufacturers pursue formulations and delivery systems that reduce technique sensitivity and integrate with digital restorative workflows. Regulatory scrutiny around biocompatibility, labeling, and manufacturing traceability has intensified, prompting more rigorous product development cycles and documentation standards.
This introduction sets the stage for an integrated exploration of how clinical practice, supply chains, and innovation pipelines converge to shape product selection and commercialization. It provides context for subsequent sections that examine transformative shifts in clinical protocols and technology adoption, the implications of trade policy changes on sourcing and procurement, and the granular segmentation and regional nuances that inform go-to-market strategies. Readers can expect evidence-based analysis grounded in practitioner priorities and operational realities rather than speculative projections.
Transformative shifts across clinical protocols, material innovation, digital workflows, and supply chain dynamics that are reshaping adhesive and sealant practice
Clinical protocols are changing rapidly as dentists pursue greater efficiency without compromising outcomes, thereby elevating demand for adhesives and sealants that reduce technique sensitivity and shorten procedure time. Concurrently, material innovation is producing hybrid chemistries and multifunctional formulations that address moisture tolerance, bond durability, and aesthetic integration. Digital workflows, including intraoral scanning and CAD/CAM restorations, are redefining how adhesives are applied and tested, encouraging suppliers to develop systems optimized for digital restorative margins and new surface treatment methods.
Supply chain dynamics and distribution models are also shifting, with manufacturers balancing centralized production and regional sourcing to manage cost and lead-time volatility. Regulatory bodies are tightening requirements for material safety and manufacturing controls, which in turn drives more rigorous validation and post-market surveillance. As a result, collaboration between clinicians, researchers, and manufacturers is intensifying to validate performance in real-world settings, accelerate clinical acceptance, and support education initiatives that shorten adoption cycles.
Cumulative impact of United States tariff adjustments in 2025 on raw material sourcing, pricing dynamics, supplier ties, and procurement for dental adhesives
Tariff actions in 2025 introduced measurable friction into procurement strategies for many dental manufacturers and distributors, prompting re-evaluation of supplier selection and cost pass-through approaches. For companies that rely on imported monomers, fillers, or specialty reagents, higher duties and administrative trade requirements elevated landed costs and complicated inventory planning. Organizations responded by diversifying supplier bases, increasing buffer stocks for critical inputs, and negotiating longer-term supply contracts with price-stabilization clauses to mitigate exposure to downstream pricing variability.
These tariff-driven changes also spurred operational adjustments in sourcing and manufacturing. Some firms accelerated nearshoring initiatives or shifted to alternative material suppliers that could meet technical specifications while presenting lower tariff risk. Procurement teams invested in deeper visibility into supplier cost structures, logistics flows, and tariff classification to optimize total cost of ownership. In parallel, product managers reassessed packaging and distribution strategies to preserve customer affordability and maintain competitive positioning amid a more complex global trade environment.
Segmentation insights into product type, material composition, end user environments, distribution paths, and application-specific clinical preferences
Effective segmentation reveals how different product architectures and end-use contexts dictate selection criteria and commercialization approaches. Based on Product Type, the landscape separates into Adhesives and Sealants; within Adhesives, clinicians choose among Etch And Rinse Adhesives, Self Etch Adhesives, and Universal Adhesives depending on substrate diversity and desired workflow simplicity, whereas Sealants split into Glass Ionomer Sealants and Resin Based Sealants driven by caries risk profile and moisture control considerations. Material Type distinctions between Glass Ionomer Based, Hybrid, and Resin Based compositions determine mechanical behavior, fluoride release potential, and surface chemistry, all of which influence clinical protocol and post-operative expectations.
End User segmentation across Academic Institutions, Hospitals, and Private Clinics surfaces divergent purchasing processes, budget cycles, and evidence requirements; academic and hospital settings often demand formal validation and broader product portfolios for training, while private clinics prioritize ease of use and value. Distribution Channel differentiators-Offline versus Online-shape accessibility and service models, with Offline delivered through Dental Supply Stores and Distributors offering local support, and Online available via E-commerce Platforms and Manufacturer Direct pathways enabling broader reach and different margin dynamics. Finally, Application-based segmentation for Caries Prevention, Orthodontic Bonding, and Restorative Bonding underscores that clinical intent drives material choice, with preventative sealants prioritizing longevity and ease of application and bonding applications emphasizing bond strength and compatibility with restorative materials. Integrating these segmentation layers enables more precise product development, tailored messaging, and targeted commercial tactics that reflect the nuanced decision rules used by practitioners across care settings.
Regional intelligence that pinpoints demand drivers, regulatory divergence, supply pressures, and clinical adoption pathways shaping dental adhesive strategies
Regional dynamics exert a pronounced influence on regulatory pathways, reimbursement patterns, and clinician preferences for adhesives and sealants. In the Americas, procurement processes emphasize cost-effectiveness and broad clinical evidence while consolidated distributor networks play a major role in channeling products to private clinics and institutional buyers. EMEA presents a more fragmented landscape where regulatory harmonization efforts coexist with localized approval requirements, creating a patchwork of compliance demands that influence market entry sequencing and labeling strategies. Asia-Pacific is characterized by rapid adoption in urban centers, a strong domestic manufacturing base in certain countries, and accelerating demand driven by broader access to dental care and preventive programs.
These regional nuances affect how companies prioritize investments in clinical trials, regulatory submissions, and localized marketing. In the Americas, emphasis on payer and clinic relationships often leads to bundled value propositions and practical training programs. In EMEA, regulatory diligence and country-specific clinical evidence become priority investments to secure market access. In Asia-Pacific, scalable manufacturing and adaptive price models are crucial to meet heterogeneous demand levels while maintaining quality and brand differentiation. Understanding regional distinctions enables more effective allocation of R&D, regulatory, and commercial resources to align with the operational realities of each geography.
Company insights on competitive positioning, R&D pipelines, partnerships, manufacturing footprints, and go-to-market tactics shaping leaders in adhesive markets
Competitive dynamics in the dental adhesives and sealants arena are defined by a blend of technical differentiation, channel relationships, and manufacturing scale. Leading firms are investing heavily in R&D pipelines to develop adhesives with improved moisture tolerance, simplified application steps, and enhanced durability under cyclic loading. Strategic partnerships and acquisitions are common as companies seek to integrate complementary technologies, expand geographic footprints, or enhance formulation capabilities. Manufacturing footprints that offer redundancy and proximity to key markets reduce lead times and provide a buffer against raw material shocks and trade disruptions.
Commercial tactics focus on bundling clinical training with product launches, expanding direct-to-clinic educational outreach, and leveraging scientific publications to build credibility among opinion leaders. Firms that combine robust clinical evidence with strong distribution relationships and responsive post-sale support tend to secure preferred status among high-volume practices and institutional buyers. Observing patent activity, regulatory filings, and collaborative research initiatives provides insight into potential shifts in competitive positioning and where incumbents or challengers are concentrating investment.
Actionable recommendations for industry leaders to enhance product development, supply chain resilience, regulatory strategy, and clinical adoption of adhesives
Industry leaders should prioritize formulation robustness and user-centered design to reduce technique sensitivity and expand use across diverse clinical settings. Investing in adhesive systems that tolerate variable moisture conditions and shorten procedural steps will lower barriers to adoption in both preventive and restorative applications. Simultaneously, strengthening supplier diversification and near-term inventory strategies will improve resilience against tariff-driven cost fluctuations and shipping disruptions. Procurement teams and product managers should collaborate to create contingency plans that balance cost, quality, and supply continuity.
Regulatory strategy must be proactive: embedding compliance, traceability, and post-market vigilance into product roadmaps avoids last-minute delays and builds trust with institutional purchasers. Commercial approaches that combine targeted clinical education, clear articulation of economic value, and flexible distribution models will accelerate uptake. For manufacturers, selective investment in local manufacturing or partnership agreements in key regions can reduce exposure to trade volatility while enabling faster response to regional product requirements. Executing these actions in a coordinated manner will strengthen competitive positioning and ensure sustainable clinical adoption.
Methodology overview of primary and secondary research, expert interviews, validation measures, and analytical frameworks that support the study's findings
The research draws on a mixed-methods approach combining primary qualitative interviews with clinicians, procurement specialists, and regulatory experts alongside a systematic review of technical literature and product dossiers. Primary interviews provided firsthand perspectives on clinical priorities, pain points in application, and procurement decision criteria, while secondary analysis clarified material science advances, regulatory developments, and published clinical results. Triangulation of these sources reduced bias and ensured that thematic conclusions reflect both practitioner experience and documented evidence.
Analytical frameworks included comparative product feature mapping, supply chain risk assessment, and stakeholder decision-pathway modeling to translate technical distinctions into commercial implications. Validation steps involved corroboration with industry experts and cross-referencing public regulatory filings and standards. This methodology ensures that insights are grounded in real-world practice and supported by multiple lines of evidence, making them actionable for R&D, regulatory, and commercial teams.
Concluding synthesis tying clinical, material, regulatory, and commercial themes into an overview of implications and priorities for dental adhesive stakeholders
The synthesis consolidates clinical imperatives, material innovations, regulatory expectations, and commercial realities into a coherent framework for stakeholders. Clinical demand is coalescing around adhesives and sealants that deliver predictable outcomes with fewer steps and greater tolerance to intraoperative variability. Material science progress is enabling hybrids and multifunctional chemistries that better balance bond strength and handling, while regulatory tightening requires more thorough validation and lifecycle documentation. Commercially, distribution and procurement strategies are adapting to digital channels and tariff-induced supply challenges, prompting firms to rethink sourcing and market entry sequencing.
Taken together, these themes suggest that success will depend on integrating product excellence with resilient supply arrangements and evidence-driven engagement with clinicians. Prioritizing interoperability with digital restorative workflows, enabling robust regulatory compliance, and aligning commercial models with regional needs will be central to capturing sustainable clinical adoption and maintaining competitive differentiation.
Please Note: PDF & Excel + Online Access - 1 Year
Introduction framing clinical needs, material science advances, regulatory evolution, and commercial dynamics shaping modern dental adhesives and sealants
The dental adhesives and sealants domain sits at the intersection of clinical demands, material science advances, and evolving regulatory frameworks, making it an essential focus for clinicians, manufacturers, and procurement leaders. Clinicians continue to demand materials that deliver reliable bonding, ease of use, and long-term clinical performance, while manufacturers pursue formulations and delivery systems that reduce technique sensitivity and integrate with digital restorative workflows. Regulatory scrutiny around biocompatibility, labeling, and manufacturing traceability has intensified, prompting more rigorous product development cycles and documentation standards.
This introduction sets the stage for an integrated exploration of how clinical practice, supply chains, and innovation pipelines converge to shape product selection and commercialization. It provides context for subsequent sections that examine transformative shifts in clinical protocols and technology adoption, the implications of trade policy changes on sourcing and procurement, and the granular segmentation and regional nuances that inform go-to-market strategies. Readers can expect evidence-based analysis grounded in practitioner priorities and operational realities rather than speculative projections.
Transformative shifts across clinical protocols, material innovation, digital workflows, and supply chain dynamics that are reshaping adhesive and sealant practice
Clinical protocols are changing rapidly as dentists pursue greater efficiency without compromising outcomes, thereby elevating demand for adhesives and sealants that reduce technique sensitivity and shorten procedure time. Concurrently, material innovation is producing hybrid chemistries and multifunctional formulations that address moisture tolerance, bond durability, and aesthetic integration. Digital workflows, including intraoral scanning and CAD/CAM restorations, are redefining how adhesives are applied and tested, encouraging suppliers to develop systems optimized for digital restorative margins and new surface treatment methods.
Supply chain dynamics and distribution models are also shifting, with manufacturers balancing centralized production and regional sourcing to manage cost and lead-time volatility. Regulatory bodies are tightening requirements for material safety and manufacturing controls, which in turn drives more rigorous validation and post-market surveillance. As a result, collaboration between clinicians, researchers, and manufacturers is intensifying to validate performance in real-world settings, accelerate clinical acceptance, and support education initiatives that shorten adoption cycles.
Cumulative impact of United States tariff adjustments in 2025 on raw material sourcing, pricing dynamics, supplier ties, and procurement for dental adhesives
Tariff actions in 2025 introduced measurable friction into procurement strategies for many dental manufacturers and distributors, prompting re-evaluation of supplier selection and cost pass-through approaches. For companies that rely on imported monomers, fillers, or specialty reagents, higher duties and administrative trade requirements elevated landed costs and complicated inventory planning. Organizations responded by diversifying supplier bases, increasing buffer stocks for critical inputs, and negotiating longer-term supply contracts with price-stabilization clauses to mitigate exposure to downstream pricing variability.
These tariff-driven changes also spurred operational adjustments in sourcing and manufacturing. Some firms accelerated nearshoring initiatives or shifted to alternative material suppliers that could meet technical specifications while presenting lower tariff risk. Procurement teams invested in deeper visibility into supplier cost structures, logistics flows, and tariff classification to optimize total cost of ownership. In parallel, product managers reassessed packaging and distribution strategies to preserve customer affordability and maintain competitive positioning amid a more complex global trade environment.
Segmentation insights into product type, material composition, end user environments, distribution paths, and application-specific clinical preferences
Effective segmentation reveals how different product architectures and end-use contexts dictate selection criteria and commercialization approaches. Based on Product Type, the landscape separates into Adhesives and Sealants; within Adhesives, clinicians choose among Etch And Rinse Adhesives, Self Etch Adhesives, and Universal Adhesives depending on substrate diversity and desired workflow simplicity, whereas Sealants split into Glass Ionomer Sealants and Resin Based Sealants driven by caries risk profile and moisture control considerations. Material Type distinctions between Glass Ionomer Based, Hybrid, and Resin Based compositions determine mechanical behavior, fluoride release potential, and surface chemistry, all of which influence clinical protocol and post-operative expectations.
End User segmentation across Academic Institutions, Hospitals, and Private Clinics surfaces divergent purchasing processes, budget cycles, and evidence requirements; academic and hospital settings often demand formal validation and broader product portfolios for training, while private clinics prioritize ease of use and value. Distribution Channel differentiators-Offline versus Online-shape accessibility and service models, with Offline delivered through Dental Supply Stores and Distributors offering local support, and Online available via E-commerce Platforms and Manufacturer Direct pathways enabling broader reach and different margin dynamics. Finally, Application-based segmentation for Caries Prevention, Orthodontic Bonding, and Restorative Bonding underscores that clinical intent drives material choice, with preventative sealants prioritizing longevity and ease of application and bonding applications emphasizing bond strength and compatibility with restorative materials. Integrating these segmentation layers enables more precise product development, tailored messaging, and targeted commercial tactics that reflect the nuanced decision rules used by practitioners across care settings.
Regional intelligence that pinpoints demand drivers, regulatory divergence, supply pressures, and clinical adoption pathways shaping dental adhesive strategies
Regional dynamics exert a pronounced influence on regulatory pathways, reimbursement patterns, and clinician preferences for adhesives and sealants. In the Americas, procurement processes emphasize cost-effectiveness and broad clinical evidence while consolidated distributor networks play a major role in channeling products to private clinics and institutional buyers. EMEA presents a more fragmented landscape where regulatory harmonization efforts coexist with localized approval requirements, creating a patchwork of compliance demands that influence market entry sequencing and labeling strategies. Asia-Pacific is characterized by rapid adoption in urban centers, a strong domestic manufacturing base in certain countries, and accelerating demand driven by broader access to dental care and preventive programs.
These regional nuances affect how companies prioritize investments in clinical trials, regulatory submissions, and localized marketing. In the Americas, emphasis on payer and clinic relationships often leads to bundled value propositions and practical training programs. In EMEA, regulatory diligence and country-specific clinical evidence become priority investments to secure market access. In Asia-Pacific, scalable manufacturing and adaptive price models are crucial to meet heterogeneous demand levels while maintaining quality and brand differentiation. Understanding regional distinctions enables more effective allocation of R&D, regulatory, and commercial resources to align with the operational realities of each geography.
Company insights on competitive positioning, R&D pipelines, partnerships, manufacturing footprints, and go-to-market tactics shaping leaders in adhesive markets
Competitive dynamics in the dental adhesives and sealants arena are defined by a blend of technical differentiation, channel relationships, and manufacturing scale. Leading firms are investing heavily in R&D pipelines to develop adhesives with improved moisture tolerance, simplified application steps, and enhanced durability under cyclic loading. Strategic partnerships and acquisitions are common as companies seek to integrate complementary technologies, expand geographic footprints, or enhance formulation capabilities. Manufacturing footprints that offer redundancy and proximity to key markets reduce lead times and provide a buffer against raw material shocks and trade disruptions.
Commercial tactics focus on bundling clinical training with product launches, expanding direct-to-clinic educational outreach, and leveraging scientific publications to build credibility among opinion leaders. Firms that combine robust clinical evidence with strong distribution relationships and responsive post-sale support tend to secure preferred status among high-volume practices and institutional buyers. Observing patent activity, regulatory filings, and collaborative research initiatives provides insight into potential shifts in competitive positioning and where incumbents or challengers are concentrating investment.
Actionable recommendations for industry leaders to enhance product development, supply chain resilience, regulatory strategy, and clinical adoption of adhesives
Industry leaders should prioritize formulation robustness and user-centered design to reduce technique sensitivity and expand use across diverse clinical settings. Investing in adhesive systems that tolerate variable moisture conditions and shorten procedural steps will lower barriers to adoption in both preventive and restorative applications. Simultaneously, strengthening supplier diversification and near-term inventory strategies will improve resilience against tariff-driven cost fluctuations and shipping disruptions. Procurement teams and product managers should collaborate to create contingency plans that balance cost, quality, and supply continuity.
Regulatory strategy must be proactive: embedding compliance, traceability, and post-market vigilance into product roadmaps avoids last-minute delays and builds trust with institutional purchasers. Commercial approaches that combine targeted clinical education, clear articulation of economic value, and flexible distribution models will accelerate uptake. For manufacturers, selective investment in local manufacturing or partnership agreements in key regions can reduce exposure to trade volatility while enabling faster response to regional product requirements. Executing these actions in a coordinated manner will strengthen competitive positioning and ensure sustainable clinical adoption.
Methodology overview of primary and secondary research, expert interviews, validation measures, and analytical frameworks that support the study's findings
The research draws on a mixed-methods approach combining primary qualitative interviews with clinicians, procurement specialists, and regulatory experts alongside a systematic review of technical literature and product dossiers. Primary interviews provided firsthand perspectives on clinical priorities, pain points in application, and procurement decision criteria, while secondary analysis clarified material science advances, regulatory developments, and published clinical results. Triangulation of these sources reduced bias and ensured that thematic conclusions reflect both practitioner experience and documented evidence.
Analytical frameworks included comparative product feature mapping, supply chain risk assessment, and stakeholder decision-pathway modeling to translate technical distinctions into commercial implications. Validation steps involved corroboration with industry experts and cross-referencing public regulatory filings and standards. This methodology ensures that insights are grounded in real-world practice and supported by multiple lines of evidence, making them actionable for R&D, regulatory, and commercial teams.
Concluding synthesis tying clinical, material, regulatory, and commercial themes into an overview of implications and priorities for dental adhesive stakeholders
The synthesis consolidates clinical imperatives, material innovations, regulatory expectations, and commercial realities into a coherent framework for stakeholders. Clinical demand is coalescing around adhesives and sealants that deliver predictable outcomes with fewer steps and greater tolerance to intraoperative variability. Material science progress is enabling hybrids and multifunctional chemistries that better balance bond strength and handling, while regulatory tightening requires more thorough validation and lifecycle documentation. Commercially, distribution and procurement strategies are adapting to digital channels and tariff-induced supply challenges, prompting firms to rethink sourcing and market entry sequencing.
Taken together, these themes suggest that success will depend on integrating product excellence with resilient supply arrangements and evidence-driven engagement with clinicians. Prioritizing interoperability with digital restorative workflows, enabling robust regulatory compliance, and aligning commercial models with regional needs will be central to capturing sustainable clinical adoption and maintaining competitive differentiation.
Please Note: PDF & Excel + Online Access - 1 Year
Table of Contents
197 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 dual-curing universal adhesives optimizing bond strength and workflow efficiency
- 5.2. Innovations in bioactive glass-containing sealants enhancing enamel remineralization and prevention
- 5.3. Growth of nanofilled adhesive formulations improving mechanical properties and microleakage resistance
- 5.4. Customized adhesive systems for CAD/CAM restorations streamlining digital dentistry workflows
- 5.5. Increasing demand for fluoride-releasing sealants offering long-term caries protection in pediatric patients
- 5.6. Emerging self-healing dental composites integrating microcapsules to repair microcracks autonomously
- 5.7. Shift toward solvent-free adhesive chemistries reducing postoperative sensitivity and improving biocompatibility
- 5.8. Surge in adoption of hydrophilic primers facilitating durable adhesion to moist dentin surfaces in vivo
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Dental Adhesives & Sealants Market, by Product Type
- 8.1. Adhesives
- 8.1.1. Etch & Rinse Adhesives
- 8.1.2. Self Etch Adhesives
- 8.1.3. Universal Adhesives
- 8.2. Sealants
- 8.2.1. Glass Ionomer Sealants
- 8.2.2. Resin Based Sealants
- 9. Dental Adhesives & Sealants Market, by Material Type
- 9.1. Glass Ionomer Based
- 9.2. Hybrid
- 9.3. Resin Based
- 10. Dental Adhesives & Sealants Market, by End User
- 10.1. Academic Institutions
- 10.2. Hospitals
- 10.3. Private Clinics
- 11. Dental Adhesives & Sealants Market, by Distribution Channel
- 11.1. Offline
- 11.2. Online
- 11.2.1. E-commerce Platforms
- 11.2.2. Manufacturer Direct
- 12. Dental Adhesives & Sealants Market, by Application
- 12.1. Caries Prevention
- 12.2. Orthodontic Bonding
- 12.3. Restorative Bonding
- 13. Dental Adhesives & Sealants 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. Dental Adhesives & Sealants Market, by Group
- 14.1. ASEAN
- 14.2. GCC
- 14.3. European Union
- 14.4. BRICS
- 14.5. G7
- 14.6. NATO
- 15. Dental Adhesives & Sealants 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. 3M Company
- 16.3.2. Dentsply Sirona Inc.
- 16.3.3. Ivoclar Vivadent AG
- 16.3.4. Kuraray Noritake Dental Inc.
- 16.3.5. GC Corporation
- 16.3.6. SDI Limited
- 16.3.7. VOCO GmbH
- 16.3.8. Ultradent Products Inc.
- 16.3.9. Mitsui Chemicals, Inc.
- 16.3.10. Pentron Clinical Technologies, LLC
- 16.3.11. Kerr Corporation
- 16.3.12. Parkell, Inc.
- 16.3.13. BISCO, Inc.
- 16.3.14. Coltene Holding AG
- 16.3.15. DMG Chemisch-Pharmazeutische Fabrik GmbH
- 16.3.16. Shofu Inc.
- 16.3.17. Pulpdent Corporation
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