Breast Reconstruction Market by Surgery Type (Bilateral, Unilateral), Product (Acellular Dermal Matrices, Breast Implants, Tissue Expanders), Reconstruction Type, Stage of Reconstruction, Age Group, End User, Application - Global Forecast 2025-2032
Description
The Breast Reconstruction Market was valued at USD 820.72 million in 2024 and is projected to grow to USD 870.13 million in 2025, with a CAGR of 6.31%, reaching USD 1,339.93 million by 2032.
Holistic introduction outlining clinical, technological, regulatory and commercial drivers that are shaping contemporary breast reconstruction decision-making and investment
This executive summary synthesizes key clinical, technological, regulatory, and commercial developments that are currently reshaping breast reconstruction practice and strategic decision-making. It draws together evidence from peer-reviewed clinical studies, regulatory notices, device approvals, and primary interviews with clinicians, procurement leads, and industry stakeholders to present an integrated view of drivers and constraints affecting surgeons, hospitals, and device manufacturers.
The following pages prioritize actionable insight for leaders focused on product development, supply chain resilience, and service-line optimization. Emphasis is placed on differentiating durable clinical advantages from transient trends so that readers can better align capital allocation and clinical training with demonstrable outcomes. Through layered analysis, this introduction sets the stage for deeper sections that address shifting clinical preferences, tariff-related operational impacts, nuanced segmentation performance across procedure types and devices, regional market dynamics, and practical recommendations designed for immediate implementation.
Compelling account of technological progress, patient expectations, and regulatory emphasis collectively reshaping clinical practice, device strategy and service delivery models
The landscape of breast reconstruction is undergoing a series of transformative shifts driven by improvements in surgical technique, device design, and patient expectations. Advances in flap reconstruction protocols and refinements in implant-based approaches have narrowed complication profiles while expanding candidacy among diverse patient cohorts. Concurrent innovations in biologic scaffolds and acellular dermal matrices are improving soft-tissue support and aesthetic outcomes, which in turn influence surgeon preference and procedure mix.
Patient-centric factors are accelerating change: heightened awareness of reconstructive options, an aging patient population with different comorbidity profiles, and the growing importance of rapid recovery pathways are prompting centers to adopt less invasive workflows and instrument sets optimized for outpatient or short-stay environments. Regulatory emphasis on post-market surveillance and real-world evidence is also reshaping commercialization strategies, prompting manufacturers to invest in registries, longitudinal outcome tracking, and value-based evidence generation. Collectively, these forces are steering resource allocation toward products and service models that demonstrate measurable improvements in patient-reported outcomes and operational efficiency.
Detailed analysis of how 2025 tariff measures have reshaped supply chains, procurement strategy, and manufacturer sourcing decisions impacting device availability and costs
The introduction of new tariffs and trade measures affecting surgical implants and biologic materials in 2025 has created a complex set of downstream effects on procurement, manufacturing strategy, and clinical practice. Supply chains for key inputs, including medical-grade silicone, biologic scaffolds, and certain sterile componentry, have experienced compositional shifts as manufacturers hedge exposure by diversifying supplier bases and accelerating nearshoring initiatives. These adjustments have implications for lead times, vendor qualification, and inventory strategy at hospitals and specialty centers.
Clinicians and purchasing teams are adapting by reassessing vendor contracts, increasing focus on total landed cost, and pursuing strategic stocking to mitigate episodic shortages. In parallel, some manufacturers are prioritizing product portfolios that offer manufacturing flexibility and lower import dependency. The combination of tariff-driven procurement pressure and ongoing clinical demand has elevated the value of supply-chain transparency, contract flexibility, and collaborative forecasting between providers and suppliers. As a result, contractual frameworks that incorporate contingency clauses, multisourcing options, and cooperative logistics planning are increasingly viewed as critical risk management tools for both providers and device companies.
In-depth segmentation insights detailing how procedure type, device class, reconstruction approach, timing, age cohorts, care settings and clinical application shape strategy
Segmentation-focused insights reveal heterogeneous dynamics across procedure types, product classes, reconstruction approaches, timing, age cohorts, care settings, and clinical applications. Based on surgery type, differentiation between bilateral and unilateral procedures affects operative planning, implant inventory needs, and expected operative times, which in turn influence hospital throughput and cost-per-case considerations. Based on product, the landscape spans acellular dermal matrices, breast implants, and tissue expanders, with breast implants further divided into saline and silicone implants and tissue expanders split between air tissue expanders and saline expanders; these product distinctions have consequences for surgeon preference, complication profiles, and long-term revision rates.
Based on reconstruction type, flap reconstruction versus implant-based reconstruction create divergent resource and training requirements, where microsurgical capabilities and perioperative support drive variation in center readiness. Based on stage of reconstruction, delayed reconstruction and immediate reconstruction involve different coordination challenges with oncology teams and influence scheduling windows and anesthesia planning. Based on age group, clinical outcomes, complication risk, and preference trends vary across cohorts of below 30, 30–50, and above 50, requiring tailored counseling and device selection. Based on end user, the profile of clinics, hospitals, and specialty surgical centers shapes adoption speed, procurement sophistication, and the capacity for bundled-care pathways. Based on application, clinical needs differ across congenital abnormalities, post-lumpectomy reconstruction, post-mastectomy reconstruction, and restoration after injury or trauma, each demanding distinct product features, imaging protocols, and multidisciplinary coordination.
Comprehensive regional analysis showing how differing reimbursement models, training ecosystems, and infrastructure drive adoption and commercialization across global territories
Regional dynamics expose differentiated pathways for adoption, reimbursement, and service model development across Americas, Europe, Middle East & Africa, and Asia-Pacific. In the Americas, concentrated centers of excellence and established private-pay pathways create opportunities for premium-technology adoption, while integrated health systems focus on standardizing clinical pathways to reduce variation and improve outcomes. Surgical training programs and high-volume academic hospitals continue to act as early adopters for advanced reconstructive techniques in this region.
In Europe, Middle East & Africa, regulatory harmonization, heterogeneous reimbursement models, and infrastructural variability drive a more cautious rollout of new device classes, with clinicians often emphasizing long-term safety data and cost-effectiveness. Adoption in the Middle East and select European markets is accelerated by investments in specialist centers, whereas lower-resource settings emphasize durability, supply reliability, and simpler device formats. In Asia-Pacific, rising healthcare investment, expanding private hospital networks, and shifting patient expectations are creating rapid uptake potential for both implant-based and flap reconstructive solutions, though success depends on local manufacturing partnerships, training capacity expansion, and alignment with evolving reimbursement frameworks.
Actionable company-level insights revealing how clinical evidence, partnership models, and supply-chain strategies are driving competitive differentiation and adoption
Leading manufacturers and service providers are advancing strategies that prioritize clinical evidence generation, surgeon engagement, and supply-chain resilience. Companies are increasingly investing in post-market registries, digital outcome platforms, and targeted clinical trials to demonstrate comparative performance for both implants and biologic adjuncts. Strategic partnerships with academic centers and surgical societies are being used to accelerate guideline inclusion and to foster surgeon familiarity through hands-on training programs and proctoring initiatives.
On the commercial front, differentiated pricing models, value-based contracting pilots, and bundled-care agreements are being piloted to align stakeholder incentives and to demonstrate the fiscal benefits of reduced complication and revision rates. Several firms are also exploring modular product lines that reduce SKU complexity for providers while maintaining clinical versatility. For new entrants and incumbents alike, the priority is to combine robust safety data with supply-chain transparency and clinician education to secure long-term adoption in both high-volume academic centers and specialty surgical settings.
Clear and pragmatic recommendations for manufacturers, providers and payers to improve evidence generation, supply resilience, tailored product strategy and value-based commercialization
To strengthen market position and clinical impact, industry leaders should prioritize four interlocking actions: strengthen clinical evidence pathways; optimize supply-chain resilience; tailor product portfolios to clinical segmentation; and align commercial models with provider incentives. Investment in longitudinal registries and pragmatic trials will yield defensible comparative effectiveness data while supporting reimbursement discussions and guideline inclusion. Simultaneously, diversifying supplier relationships, expanding nearshore manufacturing, and adopting flexible inventory strategies will mitigate exposure to tariff-related disruptions and reduce lead-time volatility.
Product strategy should mirror clinical segmentation, ensuring that implant and adjunct portfolios address the needs of bilateral and unilateral reconstructions, support both immediate and delayed timing, and accommodate age-specific considerations. Commercial teams should pilot value-based contracts and bundled payment arrangements with hospitals and specialty centers to demonstrate the economic benefits of reduced revisions and improved patient satisfaction. Finally, targeted clinician education programs and multidisciplinary pathways that integrate plastic surgery with oncology, radiology, and rehabilitation services will accelerate appropriate use and improve patient outcomes.
Robust mixed-methods research approach combining primary clinician engagement, anonymized clinical outcome data, and rigorous secondary source validation for reproducible insight
This research synthesized primary and secondary methods to ensure a balanced and verifiable evidence base. Primary inputs included structured interviews with practicing reconstructive surgeons, procurement managers, and device executives, combined with anonymized clinical outcome datasets supplied by participating centers. Secondary research comprised peer-reviewed literature, regulatory filings, device safety communications, and clinical guideline statements, with cross-validation between primary interviews and documented clinical evidence.
Data integrity protocols included standardized interview guides, double-coding of qualitative responses, and calibration meetings to reconcile conflicting inputs. Clinical outcome analysis used de-identified datasets and adherence to accepted statistical practices for comparative safety signal detection. Where applicable, regulatory timelines and approval summaries were corroborated through public authority records. Throughout the process, emphasis was placed on transparency of assumptions, clear documentation of data sources, and reproducibility of analytical steps to support confidence in the findings and inferences presented in this executive summary.
Concluding synthesis highlighting the convergence of clinical innovation, operational resilience and segmentation-led strategy as the pathway to durable market and patient outcomes
In summary, breast reconstruction is at an inflection point where technological refinement, patient expectations, and shifting procurement dynamics intersect to create opportunities and challenges for stakeholders. Clinical advances are expanding reconstructive options and improving outcomes, but realization of these benefits depends on coordinated efforts in evidence generation, clinician training, and supply-chain management. Tariff-related disruptions in 2025 have underscored the importance of procurement agility and multisourcing strategies, elevating the strategic value of logistics and supplier partnerships.
Strategic focus on segmentation-by procedure type, product class, reconstruction approach, timing, age cohort, care setting, and application-will enable manufacturers and providers to deploy resources with greater precision. Regional differentiation means that commercialization and training strategies must be tailored to local reimbursement realities and infrastructure. By integrating robust clinical evidence with resilient operations and innovative commercial models, organizations can improve patient outcomes while maintaining fiscal discipline and strategic flexibility.
Please Note: PDF & Excel + Online Access - 1 Year
Holistic introduction outlining clinical, technological, regulatory and commercial drivers that are shaping contemporary breast reconstruction decision-making and investment
This executive summary synthesizes key clinical, technological, regulatory, and commercial developments that are currently reshaping breast reconstruction practice and strategic decision-making. It draws together evidence from peer-reviewed clinical studies, regulatory notices, device approvals, and primary interviews with clinicians, procurement leads, and industry stakeholders to present an integrated view of drivers and constraints affecting surgeons, hospitals, and device manufacturers.
The following pages prioritize actionable insight for leaders focused on product development, supply chain resilience, and service-line optimization. Emphasis is placed on differentiating durable clinical advantages from transient trends so that readers can better align capital allocation and clinical training with demonstrable outcomes. Through layered analysis, this introduction sets the stage for deeper sections that address shifting clinical preferences, tariff-related operational impacts, nuanced segmentation performance across procedure types and devices, regional market dynamics, and practical recommendations designed for immediate implementation.
Compelling account of technological progress, patient expectations, and regulatory emphasis collectively reshaping clinical practice, device strategy and service delivery models
The landscape of breast reconstruction is undergoing a series of transformative shifts driven by improvements in surgical technique, device design, and patient expectations. Advances in flap reconstruction protocols and refinements in implant-based approaches have narrowed complication profiles while expanding candidacy among diverse patient cohorts. Concurrent innovations in biologic scaffolds and acellular dermal matrices are improving soft-tissue support and aesthetic outcomes, which in turn influence surgeon preference and procedure mix.
Patient-centric factors are accelerating change: heightened awareness of reconstructive options, an aging patient population with different comorbidity profiles, and the growing importance of rapid recovery pathways are prompting centers to adopt less invasive workflows and instrument sets optimized for outpatient or short-stay environments. Regulatory emphasis on post-market surveillance and real-world evidence is also reshaping commercialization strategies, prompting manufacturers to invest in registries, longitudinal outcome tracking, and value-based evidence generation. Collectively, these forces are steering resource allocation toward products and service models that demonstrate measurable improvements in patient-reported outcomes and operational efficiency.
Detailed analysis of how 2025 tariff measures have reshaped supply chains, procurement strategy, and manufacturer sourcing decisions impacting device availability and costs
The introduction of new tariffs and trade measures affecting surgical implants and biologic materials in 2025 has created a complex set of downstream effects on procurement, manufacturing strategy, and clinical practice. Supply chains for key inputs, including medical-grade silicone, biologic scaffolds, and certain sterile componentry, have experienced compositional shifts as manufacturers hedge exposure by diversifying supplier bases and accelerating nearshoring initiatives. These adjustments have implications for lead times, vendor qualification, and inventory strategy at hospitals and specialty centers.
Clinicians and purchasing teams are adapting by reassessing vendor contracts, increasing focus on total landed cost, and pursuing strategic stocking to mitigate episodic shortages. In parallel, some manufacturers are prioritizing product portfolios that offer manufacturing flexibility and lower import dependency. The combination of tariff-driven procurement pressure and ongoing clinical demand has elevated the value of supply-chain transparency, contract flexibility, and collaborative forecasting between providers and suppliers. As a result, contractual frameworks that incorporate contingency clauses, multisourcing options, and cooperative logistics planning are increasingly viewed as critical risk management tools for both providers and device companies.
In-depth segmentation insights detailing how procedure type, device class, reconstruction approach, timing, age cohorts, care settings and clinical application shape strategy
Segmentation-focused insights reveal heterogeneous dynamics across procedure types, product classes, reconstruction approaches, timing, age cohorts, care settings, and clinical applications. Based on surgery type, differentiation between bilateral and unilateral procedures affects operative planning, implant inventory needs, and expected operative times, which in turn influence hospital throughput and cost-per-case considerations. Based on product, the landscape spans acellular dermal matrices, breast implants, and tissue expanders, with breast implants further divided into saline and silicone implants and tissue expanders split between air tissue expanders and saline expanders; these product distinctions have consequences for surgeon preference, complication profiles, and long-term revision rates.
Based on reconstruction type, flap reconstruction versus implant-based reconstruction create divergent resource and training requirements, where microsurgical capabilities and perioperative support drive variation in center readiness. Based on stage of reconstruction, delayed reconstruction and immediate reconstruction involve different coordination challenges with oncology teams and influence scheduling windows and anesthesia planning. Based on age group, clinical outcomes, complication risk, and preference trends vary across cohorts of below 30, 30–50, and above 50, requiring tailored counseling and device selection. Based on end user, the profile of clinics, hospitals, and specialty surgical centers shapes adoption speed, procurement sophistication, and the capacity for bundled-care pathways. Based on application, clinical needs differ across congenital abnormalities, post-lumpectomy reconstruction, post-mastectomy reconstruction, and restoration after injury or trauma, each demanding distinct product features, imaging protocols, and multidisciplinary coordination.
Comprehensive regional analysis showing how differing reimbursement models, training ecosystems, and infrastructure drive adoption and commercialization across global territories
Regional dynamics expose differentiated pathways for adoption, reimbursement, and service model development across Americas, Europe, Middle East & Africa, and Asia-Pacific. In the Americas, concentrated centers of excellence and established private-pay pathways create opportunities for premium-technology adoption, while integrated health systems focus on standardizing clinical pathways to reduce variation and improve outcomes. Surgical training programs and high-volume academic hospitals continue to act as early adopters for advanced reconstructive techniques in this region.
In Europe, Middle East & Africa, regulatory harmonization, heterogeneous reimbursement models, and infrastructural variability drive a more cautious rollout of new device classes, with clinicians often emphasizing long-term safety data and cost-effectiveness. Adoption in the Middle East and select European markets is accelerated by investments in specialist centers, whereas lower-resource settings emphasize durability, supply reliability, and simpler device formats. In Asia-Pacific, rising healthcare investment, expanding private hospital networks, and shifting patient expectations are creating rapid uptake potential for both implant-based and flap reconstructive solutions, though success depends on local manufacturing partnerships, training capacity expansion, and alignment with evolving reimbursement frameworks.
Actionable company-level insights revealing how clinical evidence, partnership models, and supply-chain strategies are driving competitive differentiation and adoption
Leading manufacturers and service providers are advancing strategies that prioritize clinical evidence generation, surgeon engagement, and supply-chain resilience. Companies are increasingly investing in post-market registries, digital outcome platforms, and targeted clinical trials to demonstrate comparative performance for both implants and biologic adjuncts. Strategic partnerships with academic centers and surgical societies are being used to accelerate guideline inclusion and to foster surgeon familiarity through hands-on training programs and proctoring initiatives.
On the commercial front, differentiated pricing models, value-based contracting pilots, and bundled-care agreements are being piloted to align stakeholder incentives and to demonstrate the fiscal benefits of reduced complication and revision rates. Several firms are also exploring modular product lines that reduce SKU complexity for providers while maintaining clinical versatility. For new entrants and incumbents alike, the priority is to combine robust safety data with supply-chain transparency and clinician education to secure long-term adoption in both high-volume academic centers and specialty surgical settings.
Clear and pragmatic recommendations for manufacturers, providers and payers to improve evidence generation, supply resilience, tailored product strategy and value-based commercialization
To strengthen market position and clinical impact, industry leaders should prioritize four interlocking actions: strengthen clinical evidence pathways; optimize supply-chain resilience; tailor product portfolios to clinical segmentation; and align commercial models with provider incentives. Investment in longitudinal registries and pragmatic trials will yield defensible comparative effectiveness data while supporting reimbursement discussions and guideline inclusion. Simultaneously, diversifying supplier relationships, expanding nearshore manufacturing, and adopting flexible inventory strategies will mitigate exposure to tariff-related disruptions and reduce lead-time volatility.
Product strategy should mirror clinical segmentation, ensuring that implant and adjunct portfolios address the needs of bilateral and unilateral reconstructions, support both immediate and delayed timing, and accommodate age-specific considerations. Commercial teams should pilot value-based contracts and bundled payment arrangements with hospitals and specialty centers to demonstrate the economic benefits of reduced revisions and improved patient satisfaction. Finally, targeted clinician education programs and multidisciplinary pathways that integrate plastic surgery with oncology, radiology, and rehabilitation services will accelerate appropriate use and improve patient outcomes.
Robust mixed-methods research approach combining primary clinician engagement, anonymized clinical outcome data, and rigorous secondary source validation for reproducible insight
This research synthesized primary and secondary methods to ensure a balanced and verifiable evidence base. Primary inputs included structured interviews with practicing reconstructive surgeons, procurement managers, and device executives, combined with anonymized clinical outcome datasets supplied by participating centers. Secondary research comprised peer-reviewed literature, regulatory filings, device safety communications, and clinical guideline statements, with cross-validation between primary interviews and documented clinical evidence.
Data integrity protocols included standardized interview guides, double-coding of qualitative responses, and calibration meetings to reconcile conflicting inputs. Clinical outcome analysis used de-identified datasets and adherence to accepted statistical practices for comparative safety signal detection. Where applicable, regulatory timelines and approval summaries were corroborated through public authority records. Throughout the process, emphasis was placed on transparency of assumptions, clear documentation of data sources, and reproducibility of analytical steps to support confidence in the findings and inferences presented in this executive summary.
Concluding synthesis highlighting the convergence of clinical innovation, operational resilience and segmentation-led strategy as the pathway to durable market and patient outcomes
In summary, breast reconstruction is at an inflection point where technological refinement, patient expectations, and shifting procurement dynamics intersect to create opportunities and challenges for stakeholders. Clinical advances are expanding reconstructive options and improving outcomes, but realization of these benefits depends on coordinated efforts in evidence generation, clinician training, and supply-chain management. Tariff-related disruptions in 2025 have underscored the importance of procurement agility and multisourcing strategies, elevating the strategic value of logistics and supplier partnerships.
Strategic focus on segmentation-by procedure type, product class, reconstruction approach, timing, age cohort, care setting, and application-will enable manufacturers and providers to deploy resources with greater precision. Regional differentiation means that commercialization and training strategies must be tailored to local reimbursement realities and infrastructure. By integrating robust clinical evidence with resilient operations and innovative commercial models, organizations can improve patient outcomes while maintaining fiscal discipline and strategic flexibility.
Please Note: PDF & Excel + Online Access - 1 Year
Table of Contents
199 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 patient awareness driving demand for reconstructive options post-mastectomy
- 5.2. Emergence of robotic-assisted surgery facilitating precision in breast reconstruction
- 5.3. Development of bioengineered scaffolds for improved breast tissue regeneration
- 5.4. Rising focus on minimally invasive reconstructive surgeries reducing patient recovery time
- 5.5. Expanding use of acellular dermal matrices supporting implant-based reconstructions
- 5.6. Integration of regenerative medicine enhancing tissue regeneration in reconstruction
- 5.7. Growth of nipple-sparing mastectomy procedures improving aesthetic outcomes
- 5.8. Rising demand for personalized breast implants tailored to individual anatomy
- 5.9. Increasing adoption of fat grafting procedures in breast reconstruction surgeries
- 5.10. Advancements in 3D printing technology transforming breast reconstruction techniques
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Breast Reconstruction Market, by Surgery Type
- 8.1. Bilateral
- 8.2. Unilateral
- 9. Breast Reconstruction Market, by Product
- 9.1. Acellular Dermal Matrices
- 9.2. Breast Implants
- 9.2.1. Saline Breast Implants
- 9.2.2. Silicone Breast Implants
- 9.3. Tissue Expanders
- 9.3.1. Air Tissue Expander
- 9.3.2. Saline Expander
- 10. Breast Reconstruction Market, by Reconstruction Type
- 10.1. Flap Reconstruction
- 10.2. Implant-Based Reconstruction
- 11. Breast Reconstruction Market, by Stage of Reconstruction
- 11.1. Delayed Reconstruction
- 11.2. Immediate Reconstruction
- 12. Breast Reconstruction Market, by Age Group
- 12.1. 30-50
- 12.2. Above 50
- 12.3. Below 30
- 13. Breast Reconstruction Market, by End User
- 13.1. Clinics
- 13.2. Hospitals
- 13.3. Specialty Surgical Centers
- 14. Breast Reconstruction Market, by Application
- 14.1. Congenital Abnormalities
- 14.2. Post-Lumpectomy Reconstruction
- 14.3. Post-Mastectomy Reconstruction
- 14.4. Restoration After Injury or Trauma
- 15. Breast Reconstruction Market, by Region
- 15.1. Americas
- 15.1.1. North America
- 15.1.2. Latin America
- 15.2. Europe, Middle East & Africa
- 15.2.1. Europe
- 15.2.2. Middle East
- 15.2.3. Africa
- 15.3. Asia-Pacific
- 16. Breast Reconstruction Market, by Group
- 16.1. ASEAN
- 16.2. GCC
- 16.3. European Union
- 16.4. BRICS
- 16.5. G7
- 16.6. NATO
- 17. Breast Reconstruction Market, by Country
- 17.1. United States
- 17.2. Canada
- 17.3. Mexico
- 17.4. Brazil
- 17.5. United Kingdom
- 17.6. Germany
- 17.7. France
- 17.8. Russia
- 17.9. Italy
- 17.10. Spain
- 17.11. China
- 17.12. India
- 17.13. Japan
- 17.14. Australia
- 17.15. South Korea
- 18. Competitive Landscape
- 18.1. Market Share Analysis, 2024
- 18.2. FPNV Positioning Matrix, 2024
- 18.3. Competitive Analysis
- 18.3.1. 4Tissue
- 18.3.2. AbbVie Inc.
- 18.3.3. BELLASENO GmbH
- 18.3.4. Bimini Health Tech
- 18.3.5. Cerecare SAS
- 18.3.6. CollPlant Biotechnologies Ltd.
- 18.3.7. DefyGravity by Apex Medical Device Design, LLC.
- 18.3.8. Establishment Labs S.A.
- 18.3.9. Evergen
- 18.3.10. GC Aesthetics
- 18.3.11. Guangzhou Wanhe Plastic Material Co.,Ltd
- 18.3.12. Hans Biomed Co.
- 18.3.13. Implantech Associates Inc.
- 18.3.14. Integra LifeSciences Holdings Corporation
- 18.3.15. Johnson & Johnson Services, Inc.
- 18.3.16. Laboratoires Arion
- 18.3.17. Lattice Medical SAS
- 18.3.18. PMT Corporation
- 18.3.19. POLYTECH Health & Aesthetics
- 18.3.20. Sientra, Inc. by Tiger Aesthetics Medical, LLC
- 18.3.21. Symatese SAS
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