Cast Saw Devices Market by Power Source (Electric, Pneumatic), Technology (Oscillating, Reciprocating), End User, Distribution Channel - Global Forecast 2025-2032
Description
The Cast Saw Devices Market was valued at USD 208.72 million in 2024 and is projected to grow to USD 220.19 million in 2025, with a CAGR of 5.53%, reaching USD 321.15 million by 2032.
Establishing the foundational clinical and commercial context for cast saw devices by outlining roles, safety imperatives, procurement priorities, and technology drivers
Cast saw devices play a central role in modern orthopedic and wound care workflows, where precision, safety, and operational efficiency intersect. Clinicians rely on these devices to facilitate safe cast removal in ambulatory surgical centers, clinics, and hospital settings, and the device ecosystem has matured through iterative design improvements, enhanced ergonomic considerations, and focused safety features. Understanding the clinical context clarifies why device reliability, training, and maintenance protocols matter to administrators and care teams alike. Furthermore, procurement priorities increasingly emphasize lifecycle costs, supplier responsiveness, and integration with existing clinical pathways, shaping vendor selection beyond headline features and initial pricing
As technology has evolved, manufacturers have introduced alternatives in power delivery and motion profiles to address specific clinical needs. These technical variations interact with regulatory expectations and hospital risk management practices, creating differentiated value propositions. Stakeholders now require deeper evidence of safety performance and clinical utility, as well as clear support structures for training and service. This introduction frames the subsequent analysis by establishing the clinical imperatives, commercial drivers, and operational constraints that shape adoption and innovation within the cast saw device landscape
Analyzing the transformative shifts reshaping cast saw device adoption including technology convergence, clinical workflow evolution, and supply chain resilience
The cast saw device landscape is undergoing transformative shifts driven by converging pressures from technology advancement, clinical practice change, and heightened supply chain scrutiny. Newer oscillating and reciprocating mechanisms, combined with improvements in power source design, have expanded device capability while raising expectations for differentiated clinical workflows. As a result, devices that once competed primarily on price now compete on total cost of ownership, ease of use, and the strength of post-sale clinical education and servicing programs. Transitional dynamics, therefore, favor manufacturers who can demonstrate superior outcomes and streamline adoption pathways for end users
Simultaneously, regulatory emphasis on device safety and traceability has intensified, prompting suppliers to enhance labeling, user training, and service documentation. Procurement teams are responding by tightening supplier evaluation criteria and demanding more robust clinical evidence and post-market surveillance. Furthermore, digital tools and tele-support are increasingly embedded within commercial propositions, enabling remote troubleshooting and virtual training that reduce downtime and improve user competence. Taken together, these shifts are remapping competitive advantage and compelling stakeholders to reassess legacy sourcing strategies in favor of partners that offer integrated technical, clinical, and logistical value
Assessing the cumulative impact of United States tariffs enacted in 2025 on cast saw devices with focus on cost structures, sourcing adaptations, and procurement strategy shifts
Tariff actions introduced in 2025 have produced cumulative effects that ripple across sourcing strategies, vendor selection, and clinical procurement practices for cast saw devices. Manufacturers and distributors that previously relied on cross-border component sourcing found immediate pressure to reassess supplier footprints and input cost management. In response, some suppliers accelerated nearshoring initiatives or diversified component suppliers to mitigate tariff exposure, while others restructured product portfolios to preserve competitive pricing. These adjustments signaled a broader reorientation in the value chain, with an increased willingness to accept modest margin compression in exchange for supply certainty and reduced logistical risk
From the buyer perspective, hospitals, ambulatory centers, and clinics reevaluated procurement criteria by placing greater emphasis on supplier transparency and total acquisition cost rather than initial unit price alone. Contract negotiations began to include more explicit tariff pass-through clauses and contingency provisions to safeguard budgets from future trade policy shifts. Additionally, service and warranty commitments took on heightened importance because institutions prioritized reduced operational disruption. The net effect of these tariff-driven responses is a more dynamic sourcing environment where adaptability, contractual clarity, and supply-side diversification have become essential components of procurement strategies
Deriving segmentation insights for cast saw devices by synthesizing power source distinctions, technology modalities, end user profiles, and distribution channel dynamics
Segmentation analysis reveals nuanced pathways to competitive advantage by aligning product design and commercialization with specific clinical and operational needs. Examining power source distinctions, devices are categorized by electric or pneumatic modalities, with electric further delineated into battery operated and corded configurations and pneumatic divided into heavy duty and light duty classes; these differences influence portability, maintenance, and suitability across care settings. In parallel, technology distinctions separate oscillating and reciprocating mechanisms, where oscillating solutions may be refined into high frequency and low frequency types and reciprocating variants offered in fixed speed and variable speed formats; these technological choices affect cut profile, perceived safety, and clinician preference. End user segmentation highlights ambulatory surgical centers, clinics, and hospitals as distinct demand pockets, and hospitals themselves bifurcate into private and public institutions with divergent procurement dynamics and budget cycles. Distribution channels-direct sales, distributors, and online-further shape how products reach buyers and how vendors must structure sales, service, and training commitments
Taken together, these segmentation layers indicate that successful product strategies require careful alignment between device capabilities and the operational realities of target users. For example, battery operated electric devices designed for clinic use must emphasize portability and low maintenance, whereas heavy duty pneumatic offerings targeted at large hospitals should prioritize durability and robust service agreements. Meanwhile, distribution choices determine how training and post-sale support are delivered, directly affecting adoption speed and long-term customer satisfaction. By synthesizing these segmentation dimensions, manufacturers and channels can craft differentiated go-to-market approaches that resonate with provider priorities and reduce adoption friction
Comparative regional analysis of cast saw device trends with strategic insights on adoption drivers, regulatory variance, reimbursement, and supply logistics
Regional dynamics materially shape how cast saw devices are purchased, deployed, and supported in clinical practice. In the Americas, procurement patterns favor integrated supplier relationships and robust service networks, and reimbursement contexts and institutional buying power often accelerate adoption when clinical evidence supports performance improvements. Conversely, Europe, Middle East & Africa present a mosaic of regulatory regimes and reimbursement frameworks that require tailored market entry strategies, localized regulatory expertise, and adaptive pricing models. Asia-Pacific markets exhibit heterogeneity as well, with pockets of rapid adoption driven by private hospital investment alongside public systems that prioritize cost containment and standardized procurement protocols
Across these regions, logistical considerations and local manufacturing capacity influence supplier decisions on where to locate inventory and service hubs. Regulatory timelines and device registration processes vary significantly and can create lead-time differences that affect procurement windows and clinical rollout schedules. Moreover, cultural factors and clinician training expectations shape how quickly new device features are accepted in practice. Consequently, suppliers targeting multiple regions must deploy differentiated engagement strategies, invest in regional regulatory competence, and calibrate commercial models to align with local reimbursement structures and supply chain realities
Competitive company insights revealing product differentiation, distribution approaches, partnership strategies, and clinical support capabilities that shape market positioning
Competitive company dynamics in the cast saw device market revolve around product differentiation, channel execution, and the depth of clinical support offerings. Market participants that succeed tend to pair clear technical advantages-such as specific oscillating or reciprocating performance characteristics or preferred power source configurations-with robust post-sale training and service programs that reduce perceived adoption risk. Companies that invest in clinician education, structured onboarding, and rapid service response earn higher trust among procurement committees and clinical champions. At the same time, channel decisions influence market reach; firms that balance direct relationships with a calibrated distributor network and targeted online presence can optimize for both coverage and control
Partnership approaches also matter. Strategic alliances with clinical centers, training institutions, and third-party service providers extend a company’s footprint and create reference cases that aid broader adoption. Vendors that can demonstrate lower downtime, clear training curriculums, and evidence of safety performance occupy stronger negotiating positions. Finally, companies that align their commercial models with healthcare provider procurement cycles and offer flexible contracting or bundled service offerings often reduce friction in adoption, especially among large hospital systems with formalized procurement governance
Actionable recommendations for leaders to prioritize innovation, optimize procurement resilience, strengthen supply chains, and accelerate clinical adoption pathways
Industry leaders should pursue a balanced strategy that prioritizes innovation while recognizing operational realities in clinical settings. First, invest in product features that address clinician safety and ease of use, and couple technical improvements with clear training programs that minimize the learning curve. Second, strengthen procurement propositions by transparently communicating total cost implications, service commitments, and contingency plans for supply disruptions. Third, diversify supply chains to include alternate suppliers or nearshore options that reduce exposure to tariff and logistics volatility, and embed contractual mechanisms that protect both suppliers and buyers against sudden policy changes
In addition, firms should tailor distribution and pricing models to the needs of specific end users, offering portable, low-maintenance options for clinics and battery operated solutions for ambulatory settings while ensuring heavy duty, service-rich offerings for larger hospitals. Finally, develop evidence-generation plans that provide real-world data supporting device safety and workflow benefits; such evidence accelerates adoption when presented alongside targeted clinician education and a responsive service network. Executives who operationalize these recommendations will improve adoption outcomes, reduce procurement friction, and create defensible commercial advantage
Methodology overview of primary and secondary data, expert interviews, analytical approach, validation measures, and constraints that inform the cast saw device analysis
This report synthesizes primary and secondary data using a structured analytical framework to ensure credible and reproducible findings. Primary research included expert interviews with clinical users, procurement professionals, and supply chain managers, coupled with targeted vendor briefings to validate product claims and service models. Secondary sources comprised regulatory guidance documents, clinical best-practice materials, and industry literature that contextualize device function and safety expectations. Analytical approaches combined thematic synthesis of qualitative inputs with comparative evaluation of vendor capabilities and regional deployment constraints
Validation steps included triangulating interview findings with documented clinical procedures and vendor-supplied technical specifications, and applying transparent inclusion criteria for sources and evidence. Constraints are acknowledged, such as variability in regional regulatory detail and the evolving nature of trade policy, which can influence near-term commercial conditions. These methodological elements inform the integrity of the insights and provide readers with confidence in the report’s conclusions while clarifying areas where continued monitoring and additional primary research are advisable
Final synthesis distilling strategic implications and operational priorities to inform executive decision making on cast saw device adoption and deployment
The concluding synthesis integrates the preceding analysis into a cohesive set of implications and priorities that executives can operationalize. Strategic implications point to the need for an integrated value proposition that combines safe, clinician-friendly device design with comprehensive service and training. Operational priorities include supply chain diversification, transparent procurement terms, and evidence generation to substantiate claims about safety and workflow improvements. These themes recur across regions and end user types, signaling that a coordinated approach to product design, commercialization, and clinician engagement yields stronger outcomes
In practice, organizations should align commercial strategies with targeted segmentation choices and regional market dynamics, ensuring that product variants and distribution channels map to end user needs. Leadership that invests in post-sale support and clinician education will likely observe faster adoption and higher user satisfaction. The synthesis underscores the importance of resilience and adaptability in an environment shaped by policy shifts, technological progress, and evolving clinical expectations, offering a pragmatic roadmap for stakeholders seeking to make informed, executable decisions
Note: PDF & Excel + Online Access - 1 Year
Establishing the foundational clinical and commercial context for cast saw devices by outlining roles, safety imperatives, procurement priorities, and technology drivers
Cast saw devices play a central role in modern orthopedic and wound care workflows, where precision, safety, and operational efficiency intersect. Clinicians rely on these devices to facilitate safe cast removal in ambulatory surgical centers, clinics, and hospital settings, and the device ecosystem has matured through iterative design improvements, enhanced ergonomic considerations, and focused safety features. Understanding the clinical context clarifies why device reliability, training, and maintenance protocols matter to administrators and care teams alike. Furthermore, procurement priorities increasingly emphasize lifecycle costs, supplier responsiveness, and integration with existing clinical pathways, shaping vendor selection beyond headline features and initial pricing
As technology has evolved, manufacturers have introduced alternatives in power delivery and motion profiles to address specific clinical needs. These technical variations interact with regulatory expectations and hospital risk management practices, creating differentiated value propositions. Stakeholders now require deeper evidence of safety performance and clinical utility, as well as clear support structures for training and service. This introduction frames the subsequent analysis by establishing the clinical imperatives, commercial drivers, and operational constraints that shape adoption and innovation within the cast saw device landscape
Analyzing the transformative shifts reshaping cast saw device adoption including technology convergence, clinical workflow evolution, and supply chain resilience
The cast saw device landscape is undergoing transformative shifts driven by converging pressures from technology advancement, clinical practice change, and heightened supply chain scrutiny. Newer oscillating and reciprocating mechanisms, combined with improvements in power source design, have expanded device capability while raising expectations for differentiated clinical workflows. As a result, devices that once competed primarily on price now compete on total cost of ownership, ease of use, and the strength of post-sale clinical education and servicing programs. Transitional dynamics, therefore, favor manufacturers who can demonstrate superior outcomes and streamline adoption pathways for end users
Simultaneously, regulatory emphasis on device safety and traceability has intensified, prompting suppliers to enhance labeling, user training, and service documentation. Procurement teams are responding by tightening supplier evaluation criteria and demanding more robust clinical evidence and post-market surveillance. Furthermore, digital tools and tele-support are increasingly embedded within commercial propositions, enabling remote troubleshooting and virtual training that reduce downtime and improve user competence. Taken together, these shifts are remapping competitive advantage and compelling stakeholders to reassess legacy sourcing strategies in favor of partners that offer integrated technical, clinical, and logistical value
Assessing the cumulative impact of United States tariffs enacted in 2025 on cast saw devices with focus on cost structures, sourcing adaptations, and procurement strategy shifts
Tariff actions introduced in 2025 have produced cumulative effects that ripple across sourcing strategies, vendor selection, and clinical procurement practices for cast saw devices. Manufacturers and distributors that previously relied on cross-border component sourcing found immediate pressure to reassess supplier footprints and input cost management. In response, some suppliers accelerated nearshoring initiatives or diversified component suppliers to mitigate tariff exposure, while others restructured product portfolios to preserve competitive pricing. These adjustments signaled a broader reorientation in the value chain, with an increased willingness to accept modest margin compression in exchange for supply certainty and reduced logistical risk
From the buyer perspective, hospitals, ambulatory centers, and clinics reevaluated procurement criteria by placing greater emphasis on supplier transparency and total acquisition cost rather than initial unit price alone. Contract negotiations began to include more explicit tariff pass-through clauses and contingency provisions to safeguard budgets from future trade policy shifts. Additionally, service and warranty commitments took on heightened importance because institutions prioritized reduced operational disruption. The net effect of these tariff-driven responses is a more dynamic sourcing environment where adaptability, contractual clarity, and supply-side diversification have become essential components of procurement strategies
Deriving segmentation insights for cast saw devices by synthesizing power source distinctions, technology modalities, end user profiles, and distribution channel dynamics
Segmentation analysis reveals nuanced pathways to competitive advantage by aligning product design and commercialization with specific clinical and operational needs. Examining power source distinctions, devices are categorized by electric or pneumatic modalities, with electric further delineated into battery operated and corded configurations and pneumatic divided into heavy duty and light duty classes; these differences influence portability, maintenance, and suitability across care settings. In parallel, technology distinctions separate oscillating and reciprocating mechanisms, where oscillating solutions may be refined into high frequency and low frequency types and reciprocating variants offered in fixed speed and variable speed formats; these technological choices affect cut profile, perceived safety, and clinician preference. End user segmentation highlights ambulatory surgical centers, clinics, and hospitals as distinct demand pockets, and hospitals themselves bifurcate into private and public institutions with divergent procurement dynamics and budget cycles. Distribution channels-direct sales, distributors, and online-further shape how products reach buyers and how vendors must structure sales, service, and training commitments
Taken together, these segmentation layers indicate that successful product strategies require careful alignment between device capabilities and the operational realities of target users. For example, battery operated electric devices designed for clinic use must emphasize portability and low maintenance, whereas heavy duty pneumatic offerings targeted at large hospitals should prioritize durability and robust service agreements. Meanwhile, distribution choices determine how training and post-sale support are delivered, directly affecting adoption speed and long-term customer satisfaction. By synthesizing these segmentation dimensions, manufacturers and channels can craft differentiated go-to-market approaches that resonate with provider priorities and reduce adoption friction
Comparative regional analysis of cast saw device trends with strategic insights on adoption drivers, regulatory variance, reimbursement, and supply logistics
Regional dynamics materially shape how cast saw devices are purchased, deployed, and supported in clinical practice. In the Americas, procurement patterns favor integrated supplier relationships and robust service networks, and reimbursement contexts and institutional buying power often accelerate adoption when clinical evidence supports performance improvements. Conversely, Europe, Middle East & Africa present a mosaic of regulatory regimes and reimbursement frameworks that require tailored market entry strategies, localized regulatory expertise, and adaptive pricing models. Asia-Pacific markets exhibit heterogeneity as well, with pockets of rapid adoption driven by private hospital investment alongside public systems that prioritize cost containment and standardized procurement protocols
Across these regions, logistical considerations and local manufacturing capacity influence supplier decisions on where to locate inventory and service hubs. Regulatory timelines and device registration processes vary significantly and can create lead-time differences that affect procurement windows and clinical rollout schedules. Moreover, cultural factors and clinician training expectations shape how quickly new device features are accepted in practice. Consequently, suppliers targeting multiple regions must deploy differentiated engagement strategies, invest in regional regulatory competence, and calibrate commercial models to align with local reimbursement structures and supply chain realities
Competitive company insights revealing product differentiation, distribution approaches, partnership strategies, and clinical support capabilities that shape market positioning
Competitive company dynamics in the cast saw device market revolve around product differentiation, channel execution, and the depth of clinical support offerings. Market participants that succeed tend to pair clear technical advantages-such as specific oscillating or reciprocating performance characteristics or preferred power source configurations-with robust post-sale training and service programs that reduce perceived adoption risk. Companies that invest in clinician education, structured onboarding, and rapid service response earn higher trust among procurement committees and clinical champions. At the same time, channel decisions influence market reach; firms that balance direct relationships with a calibrated distributor network and targeted online presence can optimize for both coverage and control
Partnership approaches also matter. Strategic alliances with clinical centers, training institutions, and third-party service providers extend a company’s footprint and create reference cases that aid broader adoption. Vendors that can demonstrate lower downtime, clear training curriculums, and evidence of safety performance occupy stronger negotiating positions. Finally, companies that align their commercial models with healthcare provider procurement cycles and offer flexible contracting or bundled service offerings often reduce friction in adoption, especially among large hospital systems with formalized procurement governance
Actionable recommendations for leaders to prioritize innovation, optimize procurement resilience, strengthen supply chains, and accelerate clinical adoption pathways
Industry leaders should pursue a balanced strategy that prioritizes innovation while recognizing operational realities in clinical settings. First, invest in product features that address clinician safety and ease of use, and couple technical improvements with clear training programs that minimize the learning curve. Second, strengthen procurement propositions by transparently communicating total cost implications, service commitments, and contingency plans for supply disruptions. Third, diversify supply chains to include alternate suppliers or nearshore options that reduce exposure to tariff and logistics volatility, and embed contractual mechanisms that protect both suppliers and buyers against sudden policy changes
In addition, firms should tailor distribution and pricing models to the needs of specific end users, offering portable, low-maintenance options for clinics and battery operated solutions for ambulatory settings while ensuring heavy duty, service-rich offerings for larger hospitals. Finally, develop evidence-generation plans that provide real-world data supporting device safety and workflow benefits; such evidence accelerates adoption when presented alongside targeted clinician education and a responsive service network. Executives who operationalize these recommendations will improve adoption outcomes, reduce procurement friction, and create defensible commercial advantage
Methodology overview of primary and secondary data, expert interviews, analytical approach, validation measures, and constraints that inform the cast saw device analysis
This report synthesizes primary and secondary data using a structured analytical framework to ensure credible and reproducible findings. Primary research included expert interviews with clinical users, procurement professionals, and supply chain managers, coupled with targeted vendor briefings to validate product claims and service models. Secondary sources comprised regulatory guidance documents, clinical best-practice materials, and industry literature that contextualize device function and safety expectations. Analytical approaches combined thematic synthesis of qualitative inputs with comparative evaluation of vendor capabilities and regional deployment constraints
Validation steps included triangulating interview findings with documented clinical procedures and vendor-supplied technical specifications, and applying transparent inclusion criteria for sources and evidence. Constraints are acknowledged, such as variability in regional regulatory detail and the evolving nature of trade policy, which can influence near-term commercial conditions. These methodological elements inform the integrity of the insights and provide readers with confidence in the report’s conclusions while clarifying areas where continued monitoring and additional primary research are advisable
Final synthesis distilling strategic implications and operational priorities to inform executive decision making on cast saw device adoption and deployment
The concluding synthesis integrates the preceding analysis into a cohesive set of implications and priorities that executives can operationalize. Strategic implications point to the need for an integrated value proposition that combines safe, clinician-friendly device design with comprehensive service and training. Operational priorities include supply chain diversification, transparent procurement terms, and evidence generation to substantiate claims about safety and workflow improvements. These themes recur across regions and end user types, signaling that a coordinated approach to product design, commercialization, and clinician engagement yields stronger outcomes
In practice, organizations should align commercial strategies with targeted segmentation choices and regional market dynamics, ensuring that product variants and distribution channels map to end user needs. Leadership that invests in post-sale support and clinician education will likely observe faster adoption and higher user satisfaction. The synthesis underscores the importance of resilience and adaptability in an environment shaped by policy shifts, technological progress, and evolving clinical expectations, offering a pragmatic roadmap for stakeholders seeking to make informed, executable decisions
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. Increasing adoption of battery-powered cast saw devices for enhanced portability in orthopedic clinics
- 5.2. Integration of smart sensor technology to monitor blade performance and prevent patient injury
- 5.3. Rising demand for cordless cast saws with noise reduction features in pediatric care settings
- 5.4. Emergence of antimicrobial coatings on cast saw blades to reduce infection risk during procedures
- 5.5. Expansion of direct-to-consumer online sales channels for cast saw devices with telemedicine integration
- 5.6. Collaboration between manufacturers and training institutes to improve operator competency and safety compliance
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Cast Saw Devices Market, by Power Source
- 8.1. Electric
- 8.1.1. Battery Operated
- 8.1.2. Corded
- 8.2. Pneumatic
- 8.2.1. Heavy Duty
- 8.2.2. Light Duty
- 9. Cast Saw Devices Market, by Technology
- 9.1. Oscillating
- 9.1.1. High Frequency
- 9.1.2. Low Frequency
- 9.2. Reciprocating
- 9.2.1. Fixed Speed
- 9.2.2. Variable Speed
- 10. Cast Saw Devices Market, by End User
- 10.1. Ambulatory Surgical Centers
- 10.2. Clinics
- 10.3. Hospitals
- 10.3.1. Private
- 10.3.2. Public
- 11. Cast Saw Devices Market, by Distribution Channel
- 11.1. Direct Sales
- 11.2. Distributors
- 11.3. Online
- 12. Cast Saw Devices Market, by Region
- 12.1. Americas
- 12.1.1. North America
- 12.1.2. Latin America
- 12.2. Europe, Middle East & Africa
- 12.2.1. Europe
- 12.2.2. Middle East
- 12.2.3. Africa
- 12.3. Asia-Pacific
- 13. Cast Saw Devices Market, by Group
- 13.1. ASEAN
- 13.2. GCC
- 13.3. European Union
- 13.4. BRICS
- 13.5. G7
- 13.6. NATO
- 14. Cast Saw Devices Market, by Country
- 14.1. United States
- 14.2. Canada
- 14.3. Mexico
- 14.4. Brazil
- 14.5. United Kingdom
- 14.6. Germany
- 14.7. France
- 14.8. Russia
- 14.9. Italy
- 14.10. Spain
- 14.11. China
- 14.12. India
- 14.13. Japan
- 14.14. Australia
- 14.15. South Korea
- 15. Competitive Landscape
- 15.1. Market Share Analysis, 2024
- 15.2. FPNV Positioning Matrix, 2024
- 15.3. Competitive Analysis
- 15.3.1. COMED SAS
- 15.3.2. De Soutter Medical Limited by Atlas Copco
- 15.3.3. Erbrich Instrumente GmbH
- 15.3.4. Essity AB
- 15.3.5. Hanshin Medical Co., Ltd.
- 15.3.6. HEBUmedical GmbH
- 15.3.7. Koninklijke Philips N.V.
- 15.3.8. Medezine Limited
- 15.3.9. Medline Industries, LP
- 15.3.10. Medtronic PLC
- 15.3.11. OSCIMED SA
- 15.3.12. Prime Medical Inc.
- 15.3.13. RfQ-Medizintechnik GmbH & Co. KG
- 15.3.14. Rimec S.r.l.
- 15.3.15. Ross Wark Medical Ltd.
- 15.3.16. Shanghai Bojin Medical Instrument Co.,Ltd.
- 15.3.17. Stryker Corporation
- 15.3.18. Surtex Instruments Limited
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