Aesthetic Threads Market by Type (Polycaprolactone Threads, Polydioxanone Threads, Polylactic Acid Threads), Product Type (Absorbable Thread, Permanent Thread), Model, Application, End-User - Global Forecast 2025-2032
Description
The Aesthetic Threads Market was valued at USD 169.01 million in 2024 and is projected to grow to USD 183.69 million in 2025, with a CAGR of 9.27%, reaching USD 343.50 million by 2032.
Introduction to the Aesthetic Threads Market: evolving clinical preferences, technological advancements, and stakeholder expectations shaping procedural trends
This executive summary introduces the aesthetic threads landscape at a pivotal moment characterized by accelerating clinical interest, iterative material science advancements, and increasingly sophisticated care pathways. Practitioners and procurement professionals are navigating a convergence of factors: patient preferences that prioritize minimally invasive options, clinicians seeking reproducible outcomes that balance lift with natural tissue response, and manufacturers focused on delivering differentiated clinical evidence and device performance. As a result, stakeholder decisions are shifting from single-dimension selection criteria toward integrated assessments that weigh product composition, clinical model compatibility, and long-term safety profiles.
Moreover, the introduction frames how ecosystem actors-clinics, dermatology centers, and hospital departments-are adapting their service offerings and operational protocols. In parallel, regulatory engagement and payer considerations are prompting more rigorous data collection and post-market surveillance. Taken together, these developments establish the context for the sections that follow, where structural changes, tariff impacts, segmentation implications, regional dynamics, competitive behaviors, recommendations, and methodological rigor are examined to guide leaders in aligning commercial strategy with clinical realities.
Transformative shifts redefining procedural aesthetics with absorbable thread innovation, patient demand dynamics, regulatory evolution, and care pathway integration
The landscape for aesthetic threads is experiencing transformative shifts driven by three interrelated vectors: materials innovation, clinical practice evolution, and stakeholder expectations for evidence. On the materials front, incremental improvements in polymer chemistry and thread design have enabled finer control over biodegradation profiles and mechanical characteristics, which in turn broaden clinician choice for matching thread properties to patient anatomy and treatment intent. Consequently, clinicians are experimenting with hybrid procedural protocols that combine threads with adjunctive modalities to enhance collagen stimulation and durable contouring results.
In clinical practice, there is an observable migration from isolated cosmetic procedures to integrated care pathways that emphasize predictable recovery, measurable outcomes, and clear patient education. As such, clinics and medspas are investing in training, standardized outcome measures, and selective case triage to maintain safety and reputation. Meanwhile, regulatory authorities and institutional procurement bodies are encouraging higher standards for clinical data, which incentivizes manufacturers to prioritize robust evidence generation. Taken together, these shifts are not incremental; they represent a reframing of how products are evaluated and adopted, accelerating alignment between clinical need and device innovation.
Assessing cumulative effects of United States tariff changes in 2025 on procurement, supply continuity, manufacturing recalibration, and clinical delivery
Tariff adjustments enacted by the United States in 2025 have exerted a multifaceted influence on the aesthetic threads value chain, prompting immediate operational recalibrations and prompting strategic reappraisals of supply continuity. Importantly, procurement teams have had to reassess sourcing strategies to mitigate cost volatility and maintain predictable clinical inventories, which in turn has encouraged the exploration of alternative suppliers, resourcing models, and buffer-stocking practices. At the manufacturing level, some firms have accelerated localization, dual-sourcing, or contract manufacturing agreements to reduce exposure to cross-border tariff shifts and to preserve timely fulfillment for clinical customers.
Furthermore, the tariff environment has increased the emphasis on total landed cost and value engineering rather than headline unit price alone. This has intensified conversations around reformulation, packaging optimization, and logistical efficiency. Clinicians and institutions are responding by tightening purchasing approval criteria and requiring clearer documentation of product provenance and quality controls. While tariffs are only one element among many pressures, their effect has been to magnify the importance of resilient distribution, transparent supplier relationships, and proactive stakeholder communication throughout the adoption lifecycle.
Key segmentation insights revealing how thread composition, product permanence, clinical models, targeted applications, and end-user profiles shape adoption
Segmentation analysis reveals nuanced adoption patterns across thread types, product permanence, clinical models, application areas, and end-user settings. Based on Type, the market is studied across Polycaprolactone Threads, Polydioxanone Threads, and Polylactic Acid Threads, with Polydioxanone Threads further differentiated into PDO Cog Threads, PDO Mono Threads, and PDO Screw Threads to reflect how procedural technique and tissue interaction drive clinician choice. Product Type distinctions between Absorbable Thread and Permanent Thread inform conversations about patient expectations, longevity of results, and regulatory scrutiny, with absorbable constructs frequently favored for their safety profile and reversible nature.
In terms of Model, the bifurcation into Rejuvenating Thread and Suspension Thread captures differing objectives: one emphasizes collagen stimulation and textural improvement while the other prioritizes mechanical lift. Applications span Body Contouring, Collagen Stimulation, Facial Lifting & Contouring, and Neck Rejuvenation, each presenting discrete anatomical challenges and training requirements. Finally, End-User segmentation covers Beauty Clinics & Medspas, Dermatology Centers, and Hospitals, which vary in procedural volume, clinical governance, and the complexity of cases they manage. Together, these segmentation lenses create a composite picture that informs product development, training programs, and commercialization strategies aligned with real-world clinical workflows.
Strategic regional insights highlighting growth drivers, clinical trends, regulatory nuances, and supply chain strengths across Americas, EMEA, and Asia-Pacific markets
Regional dynamics shape both demand drivers and operational approaches across the Americas, Europe, Middle East & Africa, and Asia-Pacific, each exhibiting distinct clinical cultures, regulatory frameworks, and supply chain characteristics. In the Americas, clinician entrepreneurship and consumer willingness to adopt minimally invasive procedures support rapid diffusion of novel thread formats, while institutional purchasers are increasingly focused on procurement transparency and lifecycle performance. Moving toward Europe, Middle East & Africa, heterogeneous regulatory regimes and varying reimbursement environments create a patchwork of adoption tempos, which rewards manufacturers who can demonstrate consistent safety data and provide localized support for training and regulatory navigation.
Asia-Pacific presents a diverse set of mature and emerging markets, characterized by high procedure volumes in urban centers, proactive clinician training ecosystems, and strong interest in combinations of threads with energy-based devices. Across regions, supply chain resilience and localized clinical education are recurrent themes; companies that align distribution models with regional regulatory expectations and clinician training preferences are better positioned to capture sustained engagement. Consequently, regional strategies must balance global standards with tailored approaches to training, regulatory support, and patient communication.
Competitive company landscape analysis emphasizing product innovation, clinical evidence generation, and strategic partnerships across industry players
Competitive dynamics emphasize differentiated product portfolios, evidence generation, strategic partnerships, and operational excellence. Leading companies are prioritizing rigorous clinical studies that demonstrate longitudinal safety and procedure-specific outcomes, thereby enabling surgeons and dermatologists to make informed choices based on comparative evidence rather than marketing claims alone. In addition, product innovation is increasingly framed by ease-of-use, reproducibility across a range of anatomies, and compatibility with adjunctive therapies, which supports broader clinical adoption and practitioner confidence.
Strategic partnerships with training institutions, key opinion leaders, and regional distributors serve as important accelerants for market entry and clinician credentialing. Moreover, manufacturers that can demonstrate robust quality systems and transparent supply chains reduce perceived adoption risk for larger purchasing entities. Taken together, these behaviors underscore a competitive environment where sustained investment in clinical validation, education, and supply reliability is often more decisive than short-term promotional tactics.
Actionable recommendations for industry leaders to accelerate clinical adoption, streamline procurement, strengthen evidence portfolios, and improve supply resilience
Industry leaders can pursue a set of coordinated actions to accelerate meaningful adoption while managing operational risk. First, investing in targeted clinical evidence that aligns with the priorities of surgeons, dermatologists, and hospital committees will materially lower barriers to acceptance and institutional approval. Second, developing modular training curricula that combine hands-on skill development with standardized outcome tracking will improve procedural consistency and patient satisfaction. Third, procurement teams should be engaged early through transparent total-cost discussions, including logistics and warranty terms, to avoid procurement delays and minimize stock disruptions.
Additionally, diversifying manufacturing and distribution channels-whether through regional contract manufacturing, strategic distributor partnerships, or dual-sourced components-can materially improve supply resilience. Finally, aligning marketing and medical affairs communications to emphasize clinical endpoints, safety data, and realistic patient expectations will foster trust among clinicians and patients alike. By implementing these integrated actions, leaders can convert insight into sustained clinical and commercial momentum.
Robust research methodology explaining data sources, stakeholder engagement, evidence grading, and analytical approaches used to derive actionable insights
The research methodology underpinning this study combines primary stakeholder engagement, systematic evidence appraisal, and triangulated data synthesis to ensure robust and reproducible findings. Primary interviews were conducted with clinicians, procurement professionals, and distribution partners to capture lived experience, procedural preferences, and operational constraints. These qualitative inputs were then triangulated with peer-reviewed clinical literature, regulatory filings, and product technical specifications to generate a holistic view of performance characteristics and safety considerations.
Evidence was graded according to clinical relevance and study design rigor, and analytical approaches prioritized scenario-based sensitivity checks to reflect realistic pathways for adoption and supply management. Where appropriate, comparative device performance was assessed through cross-study frameworks that normalize endpoints to common clinical measures. Throughout the process, attention was given to transparency of assumptions, documentation of interview protocols, and the reproducibility of analytical steps so that decision-makers can trace findings back to source material and adapt them to their organizational context.
Conclusion synthesizing strategic opportunities, operational challenges, and the path forward for clinical adoption, innovation, and cross-sector collaboration
The conclusion synthesizes strategic opportunities and operational imperatives for organizations operating within the aesthetic threads ecosystem. Opportunities exist in aligning product design with clinician workflows, expanding clinician education to reduce variation in technique, and cultivating evidence that answers the specific questions of institutional buyers. Operationally, supply resilience and transparent procurement dialogue remain critical priorities, especially in light of trade policy shifts and evolving distribution channels. Cross-sector collaboration-between manufacturers, clinical trainers, and regulatory stakeholders-will be pivotal in creating standardized outcome measures and shared safety registries.
Looking ahead, organizations that focus on integrated value propositions-combining compelling clinical data, scalable training, and reliable supply models-are best positioned to navigate complexity and build durable adoption pathways. By synthesizing technical innovation with pragmatic operational planning, stakeholders can convert present disruption into long-term clinical and commercial gains.
Note: PDF & Excel + Online Access - 1 Year
Introduction to the Aesthetic Threads Market: evolving clinical preferences, technological advancements, and stakeholder expectations shaping procedural trends
This executive summary introduces the aesthetic threads landscape at a pivotal moment characterized by accelerating clinical interest, iterative material science advancements, and increasingly sophisticated care pathways. Practitioners and procurement professionals are navigating a convergence of factors: patient preferences that prioritize minimally invasive options, clinicians seeking reproducible outcomes that balance lift with natural tissue response, and manufacturers focused on delivering differentiated clinical evidence and device performance. As a result, stakeholder decisions are shifting from single-dimension selection criteria toward integrated assessments that weigh product composition, clinical model compatibility, and long-term safety profiles.
Moreover, the introduction frames how ecosystem actors-clinics, dermatology centers, and hospital departments-are adapting their service offerings and operational protocols. In parallel, regulatory engagement and payer considerations are prompting more rigorous data collection and post-market surveillance. Taken together, these developments establish the context for the sections that follow, where structural changes, tariff impacts, segmentation implications, regional dynamics, competitive behaviors, recommendations, and methodological rigor are examined to guide leaders in aligning commercial strategy with clinical realities.
Transformative shifts redefining procedural aesthetics with absorbable thread innovation, patient demand dynamics, regulatory evolution, and care pathway integration
The landscape for aesthetic threads is experiencing transformative shifts driven by three interrelated vectors: materials innovation, clinical practice evolution, and stakeholder expectations for evidence. On the materials front, incremental improvements in polymer chemistry and thread design have enabled finer control over biodegradation profiles and mechanical characteristics, which in turn broaden clinician choice for matching thread properties to patient anatomy and treatment intent. Consequently, clinicians are experimenting with hybrid procedural protocols that combine threads with adjunctive modalities to enhance collagen stimulation and durable contouring results.
In clinical practice, there is an observable migration from isolated cosmetic procedures to integrated care pathways that emphasize predictable recovery, measurable outcomes, and clear patient education. As such, clinics and medspas are investing in training, standardized outcome measures, and selective case triage to maintain safety and reputation. Meanwhile, regulatory authorities and institutional procurement bodies are encouraging higher standards for clinical data, which incentivizes manufacturers to prioritize robust evidence generation. Taken together, these shifts are not incremental; they represent a reframing of how products are evaluated and adopted, accelerating alignment between clinical need and device innovation.
Assessing cumulative effects of United States tariff changes in 2025 on procurement, supply continuity, manufacturing recalibration, and clinical delivery
Tariff adjustments enacted by the United States in 2025 have exerted a multifaceted influence on the aesthetic threads value chain, prompting immediate operational recalibrations and prompting strategic reappraisals of supply continuity. Importantly, procurement teams have had to reassess sourcing strategies to mitigate cost volatility and maintain predictable clinical inventories, which in turn has encouraged the exploration of alternative suppliers, resourcing models, and buffer-stocking practices. At the manufacturing level, some firms have accelerated localization, dual-sourcing, or contract manufacturing agreements to reduce exposure to cross-border tariff shifts and to preserve timely fulfillment for clinical customers.
Furthermore, the tariff environment has increased the emphasis on total landed cost and value engineering rather than headline unit price alone. This has intensified conversations around reformulation, packaging optimization, and logistical efficiency. Clinicians and institutions are responding by tightening purchasing approval criteria and requiring clearer documentation of product provenance and quality controls. While tariffs are only one element among many pressures, their effect has been to magnify the importance of resilient distribution, transparent supplier relationships, and proactive stakeholder communication throughout the adoption lifecycle.
Key segmentation insights revealing how thread composition, product permanence, clinical models, targeted applications, and end-user profiles shape adoption
Segmentation analysis reveals nuanced adoption patterns across thread types, product permanence, clinical models, application areas, and end-user settings. Based on Type, the market is studied across Polycaprolactone Threads, Polydioxanone Threads, and Polylactic Acid Threads, with Polydioxanone Threads further differentiated into PDO Cog Threads, PDO Mono Threads, and PDO Screw Threads to reflect how procedural technique and tissue interaction drive clinician choice. Product Type distinctions between Absorbable Thread and Permanent Thread inform conversations about patient expectations, longevity of results, and regulatory scrutiny, with absorbable constructs frequently favored for their safety profile and reversible nature.
In terms of Model, the bifurcation into Rejuvenating Thread and Suspension Thread captures differing objectives: one emphasizes collagen stimulation and textural improvement while the other prioritizes mechanical lift. Applications span Body Contouring, Collagen Stimulation, Facial Lifting & Contouring, and Neck Rejuvenation, each presenting discrete anatomical challenges and training requirements. Finally, End-User segmentation covers Beauty Clinics & Medspas, Dermatology Centers, and Hospitals, which vary in procedural volume, clinical governance, and the complexity of cases they manage. Together, these segmentation lenses create a composite picture that informs product development, training programs, and commercialization strategies aligned with real-world clinical workflows.
Strategic regional insights highlighting growth drivers, clinical trends, regulatory nuances, and supply chain strengths across Americas, EMEA, and Asia-Pacific markets
Regional dynamics shape both demand drivers and operational approaches across the Americas, Europe, Middle East & Africa, and Asia-Pacific, each exhibiting distinct clinical cultures, regulatory frameworks, and supply chain characteristics. In the Americas, clinician entrepreneurship and consumer willingness to adopt minimally invasive procedures support rapid diffusion of novel thread formats, while institutional purchasers are increasingly focused on procurement transparency and lifecycle performance. Moving toward Europe, Middle East & Africa, heterogeneous regulatory regimes and varying reimbursement environments create a patchwork of adoption tempos, which rewards manufacturers who can demonstrate consistent safety data and provide localized support for training and regulatory navigation.
Asia-Pacific presents a diverse set of mature and emerging markets, characterized by high procedure volumes in urban centers, proactive clinician training ecosystems, and strong interest in combinations of threads with energy-based devices. Across regions, supply chain resilience and localized clinical education are recurrent themes; companies that align distribution models with regional regulatory expectations and clinician training preferences are better positioned to capture sustained engagement. Consequently, regional strategies must balance global standards with tailored approaches to training, regulatory support, and patient communication.
Competitive company landscape analysis emphasizing product innovation, clinical evidence generation, and strategic partnerships across industry players
Competitive dynamics emphasize differentiated product portfolios, evidence generation, strategic partnerships, and operational excellence. Leading companies are prioritizing rigorous clinical studies that demonstrate longitudinal safety and procedure-specific outcomes, thereby enabling surgeons and dermatologists to make informed choices based on comparative evidence rather than marketing claims alone. In addition, product innovation is increasingly framed by ease-of-use, reproducibility across a range of anatomies, and compatibility with adjunctive therapies, which supports broader clinical adoption and practitioner confidence.
Strategic partnerships with training institutions, key opinion leaders, and regional distributors serve as important accelerants for market entry and clinician credentialing. Moreover, manufacturers that can demonstrate robust quality systems and transparent supply chains reduce perceived adoption risk for larger purchasing entities. Taken together, these behaviors underscore a competitive environment where sustained investment in clinical validation, education, and supply reliability is often more decisive than short-term promotional tactics.
Actionable recommendations for industry leaders to accelerate clinical adoption, streamline procurement, strengthen evidence portfolios, and improve supply resilience
Industry leaders can pursue a set of coordinated actions to accelerate meaningful adoption while managing operational risk. First, investing in targeted clinical evidence that aligns with the priorities of surgeons, dermatologists, and hospital committees will materially lower barriers to acceptance and institutional approval. Second, developing modular training curricula that combine hands-on skill development with standardized outcome tracking will improve procedural consistency and patient satisfaction. Third, procurement teams should be engaged early through transparent total-cost discussions, including logistics and warranty terms, to avoid procurement delays and minimize stock disruptions.
Additionally, diversifying manufacturing and distribution channels-whether through regional contract manufacturing, strategic distributor partnerships, or dual-sourced components-can materially improve supply resilience. Finally, aligning marketing and medical affairs communications to emphasize clinical endpoints, safety data, and realistic patient expectations will foster trust among clinicians and patients alike. By implementing these integrated actions, leaders can convert insight into sustained clinical and commercial momentum.
Robust research methodology explaining data sources, stakeholder engagement, evidence grading, and analytical approaches used to derive actionable insights
The research methodology underpinning this study combines primary stakeholder engagement, systematic evidence appraisal, and triangulated data synthesis to ensure robust and reproducible findings. Primary interviews were conducted with clinicians, procurement professionals, and distribution partners to capture lived experience, procedural preferences, and operational constraints. These qualitative inputs were then triangulated with peer-reviewed clinical literature, regulatory filings, and product technical specifications to generate a holistic view of performance characteristics and safety considerations.
Evidence was graded according to clinical relevance and study design rigor, and analytical approaches prioritized scenario-based sensitivity checks to reflect realistic pathways for adoption and supply management. Where appropriate, comparative device performance was assessed through cross-study frameworks that normalize endpoints to common clinical measures. Throughout the process, attention was given to transparency of assumptions, documentation of interview protocols, and the reproducibility of analytical steps so that decision-makers can trace findings back to source material and adapt them to their organizational context.
Conclusion synthesizing strategic opportunities, operational challenges, and the path forward for clinical adoption, innovation, and cross-sector collaboration
The conclusion synthesizes strategic opportunities and operational imperatives for organizations operating within the aesthetic threads ecosystem. Opportunities exist in aligning product design with clinician workflows, expanding clinician education to reduce variation in technique, and cultivating evidence that answers the specific questions of institutional buyers. Operationally, supply resilience and transparent procurement dialogue remain critical priorities, especially in light of trade policy shifts and evolving distribution channels. Cross-sector collaboration-between manufacturers, clinical trainers, and regulatory stakeholders-will be pivotal in creating standardized outcome measures and shared safety registries.
Looking ahead, organizations that focus on integrated value propositions-combining compelling clinical data, scalable training, and reliable supply models-are best positioned to navigate complexity and build durable adoption pathways. By synthesizing technical innovation with pragmatic operational planning, stakeholders can convert present disruption into long-term clinical and commercial gains.
Note: PDF & Excel + Online Access - 1 Year
Table of Contents
192 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. Growing demand for minimally invasive absorbable suture materials with proven collagen stimulation efficacy
- 5.2. Surge in patient preference for virtual consultation and remote monitoring in aesthetic thread procedures
- 5.3. Rising influence of social media tutorials and influencer partnerships on shaping aesthetic thread treatment trends
- 5.4. Advancements in thread lift technology integrating biocompatible polymers and nanocoated delivery systems
- 5.5. Increasing regulatory scrutiny and standardized training requirements for aesthetic thread practitioners globally
- 5.6. Emergence of male aesthetic thread procedures driven by rising awareness of minimally invasive facial rejuvenation options
- 5.7. Integration of 3D imaging and augmented reality for personalized treatment planning in aesthetic thread lift procedures
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Aesthetic Threads Market, by Type
- 8.1. Polycaprolactone Threads
- 8.2. Polydioxanone Threads
- 8.2.1. PDO Cog Threads
- 8.2.2. PDO Mono Threads
- 8.2.3. PDO Screw Threads
- 8.3. Polylactic Acid Threads
- 9. Aesthetic Threads Market, by Product Type
- 9.1. Absorbable Thread
- 9.2. Permanent Thread
- 10. Aesthetic Threads Market, by Model
- 10.1. Rejuvenating Thread
- 10.2. Suspension Thread
- 11. Aesthetic Threads Market, by Application
- 11.1. Body Contouring
- 11.2. Collagen Stimulation
- 11.3. Facial Lifting & Contouring
- 11.4. Neck Rejuvenation
- 12. Aesthetic Threads Market, by End-User
- 12.1. Beauty Clinics & Medspas
- 12.2. Dermatology Centers
- 12.3. Hospitals
- 13. Aesthetic Threads 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. Aesthetic Threads Market, by Group
- 14.1. ASEAN
- 14.2. GCC
- 14.3. European Union
- 14.4. BRICS
- 14.5. G7
- 14.6. NATO
- 15. Aesthetic Threads 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. Aesthetic Experts Labs Ltd.
- 16.3.2. Allergan Aesthetics by AbbVie Inc.
- 16.3.3. ApolloMed Innovations
- 16.3.4. Aptos LLC
- 16.3.5. BISTOOL
- 16.3.6. Croma-Pharma GmbH
- 16.3.7. Dermax Co., Ltd.
- 16.3.8. Diaminy PDO Threads
- 16.3.9. Diamond Biotechnology Co., Ltd.
- 16.3.10. Ewell Medical
- 16.3.11. Exclusive Med Aesthetics
- 16.3.12. Hans Biomed Co., Ltd.
- 16.3.13. Healux Co., Ltd.
- 16.3.14. Hebei Ulike Technology Co.,Ltd.
- 16.3.15. HUGEL, Inc.
- 16.3.16. Illari Threads, LLC
- 16.3.17. Koru Pharma Co., LTD.
- 16.3.18. Les Encres, LLC
- 16.3.19. LUXEFACE&LUXEBODY
- 16.3.20. Medical Aesthetic Group
- 16.3.21. Medical Sparx
- 16.3.22. META BIOMED CO,. LTD.
- 16.3.23. Metro Korea Co., Ltd.
- 16.3.24. N-Finders
- 16.3.25. PDO Max
- 16.3.26. Shanghai Yastrid Industry Co.,Ltd.
- 16.3.27. Shangyang Medical
- 16.3.28. Sinclair Pharma Ltd. by Huadong Medicine Company Limited
- 16.3.29. Spring Thread
- 16.3.30. The Menarini Group
- 16.3.31. TM GLOBAL Co,. Ltd.
- 16.3.32. V Soft Lift AB
- 16.3.33. Viola Threads
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