시장보고서
상품코드
1839048

근시 및 노안 치료 시장 : 치료 유형, 연령층, 질환 유형, 유통 채널별 - 세계 예측(2025-2032년)

Myopia & Presbyopia Treatment Market by Treatment Type, Age Group, Disease Type, Distribution Channel - Global Forecast 2025-2032

발행일: | 리서치사: 360iResearch | 페이지 정보: 영문 198 Pages | 배송안내 : 1-2일 (영업일 기준)

    
    
    




■ 보고서에 따라 최신 정보로 업데이트하여 보내드립니다. 배송일정은 문의해 주시기 바랍니다.

근시 및 노안 치료 시장은 2032년까지 연평균 복합 성장률(CAGR) 9.49%로 457억 7,000만 달러에 이를 것으로 예측됩니다.

주요 시장 통계
기준 연도 : 2024년 221억 4,000만 달러
추정 연도 : 2025년 241억 3,000만 달러
예측 연도 : 2032년 457억 7,000만 달러
CAGR(%) 9.49%

굴절교정 치료의 제공과 상업화를 재구성하고 있는 임상 혁신, 수렴하는 임상 혁신, 인구통계학적 압력, 환자들의 기대에 대한 전략적 개요

굴절 교정 치료를 둘러싼 환경은 동시 다발적인 임상 혁신, 인구 통계학적 변화, 환자들의 기대치 변화에 힘입어 빠르게 변화하고 있습니다. 광학 기기, 수술 기법, 약리학적 개입의 발전은 근시와 노안 모두에 대한 전통적인 치료 경로를 재구성하고 있으며, 치료 제공 및 유통 채널의 변화는 환자가 솔루션에 접근하는 방식을 변화시키고 있습니다. 임상의들은 보다 광범위한 치료 옵션에 적응하고 있으며, 수년간의 수술적 접근법과 새롭게 등장한 비침습적 및 약리학적 도구의 균형을 맞추고 있습니다.

동시에 환자들의 요구도 점점 더 미묘해지고 있습니다. 디지털 네이티브 집단은 편리함과 개인화된 선택권을 기대하며, 노년층은 일상 업무에서 기능적 시력을 유지할 수 있는 솔루션을 원합니다. 이러한 변화에 따라 제조업체, 서비스 제공업체, 지불자는 제품 설계, 임상 교육, 상환에 대한 대화를 다시 생각해야 합니다. 임상적 근거 창출과 상업적 채택 사이의 상호 작용이 점점 더 중요해지고 있으며, 유효성 데이터와 운영상의 타당성 및 환자 경험을 일치시킬 수 있는 이해관계자는 경쟁 우위를 확보할 수 있을 것으로 보입니다. 즉, 본 소개서는 굴절교정 치료의 단기적 우선순위와 장기적 가치 창출을 결정하는 임상적, 규제적, 상업적 벡터를 전략적으로 평가할 수 있는 발판을 마련할 것입니다.

수렴적 임상적 혁신, 디지털 참여, 치료 경로 재구성이 굴절교정 의료의 치료 접근법과 시장 역학을 빠르게 재정의하는 방법

지난 몇 년 동안 굴절이상 치료를 재정의하기 위해 임상, 기술 및 환자 경로에 혁신적인 변화가 일어나고 있습니다. 임상적 측면에서는 수술 기법과 안구 내 렌즈 광학계가 진화하여 노안에 대처하고 시력의 질을 개선하고 시력 장애를 완화할 수 있게 됨에 따라, 저침습적이고 렌즈를 이용한 치료법의 채택이 가속화되고 있습니다. 동시에 근시 관리는 예방적 권고에서 구조화된 치료 알고리즘으로 이동하고 있으며, 약리학적 옵션과 젊은 환자들을 위한 맞춤형 행동 중재가 널리 받아들여지고 있습니다. 이러한 임상적 발전은 치료 계층구조를 바꾸고, 안과, 검안학, 1차의료 간의 새로운 다학제적 협업을 촉진하고 있습니다.

상업적으로, 디지털 채널과 소비자 직접 판매 모델은 환자의 인식과 수요를 증가시켜 전통적인 유통 모델과 임상 모델의 적응을 강요하고 있습니다. 장비 제조업체와 서비스 제공업체들은 원격 검진, 순응도 모니터링, 수술 후 관리를 위한 디지털 도구에 투자하고 있습니다. 결과의 질과 장기적 안전성에 대한 규제 당국의 관심이 높아짐에 따라 확고한 실제 임상 증거에 대한 필요성이 가속화되고 있습니다. 그 결과, 조직의 우선순위에는 임상적 증거 생성 강화, 디지털 참여 역량 강화, 전체 진료 환경에서 신뢰할 수 있는 제품 접근을 보장하기 위한 공급망 탄력성 강화 등이 포함되었습니다.

무역 정책 변화가 굴절교정 의료 이해관계자 전반의 조달, 공급망, 전략적 조달 결정에 미치는 실질적 영향 평가

2025년 전후로 시행된 관세 정책 변경과 무역 조치로 인해 굴절교정 치료 생태계공급망, 조달, 가격 설정에 새로운 고려사항이 도입되었습니다. 관세로 인해 수술기구, 렌즈, 보조기구의 수입비용이 상승하면 구매자와 제조업체는 즉시 투입비용과 조달 일정에 대한 압박을 받게 됩니다. 이러한 무역 충격에 대한 역사적으로 관찰된 반응으로는 전략적 조달 조정, 재고 버퍼 증가, 공급업체 다변화 가속화 등이 있으며, 이 모든 것이 안경원 및 안경 소매점을 지원하는 유통 네트워크를 재구성할 가능성이 있습니다.

보다 구체적으로, 관세로 인한 비용 압력은 종종 제조업체가 국경 간 관세의 영향을 줄이고 가격 경쟁력을 유지하기 위해 주요 부품의 현지 조립 및 니어쇼어링을 평가하게 합니다. 의료 서비스 제공업체는 구매 시기를 조정하고, 서비스 계약을 재협상하고, 안정적인 공급망을 갖춘 제품을 우선적으로 구매하는 방식으로 대응합니다. 지불자와 조달 기관은 비용 효율성 및 총소유비용에 대한 모니터링을 강화하고, 의료기기 공급업체가 임상적 성과와 장기적 가치를 강조하도록 유도할 수 있습니다. 전반적으로 관세 관련 조치의 누적 영향은 공급망 탄력성, 계약 유연성, 비용 구조의 투명성 향상을 촉진하고 일시적인 조정이 아닌 지속적인 전략적 전환을 촉진하는 것입니다.

전략적으로 실행 가능한 세분화 분석을 통해 치료 방식, 환자군, 질병 카테고리, 유통 채널을 조정하여 임상 도입 및 상업적 영향력을 최적화합니다.

통찰력 있는 세분화를 통해 이해관계자들은 각 코호트 및 치료 경로의 명확한 니즈에 맞게 제품 개발, 임상시험 및 시장 개발 전략을 조정할 수 있습니다. 치료 유형별로 보면 백내장 수술, 교정렌즈, 이식렌즈, 수술적 치료가 있으며, 교정렌즈는 다시 콘택트렌즈, 안경, 다초점렌즈, 난시교정렌즈로 세분화되어 있습니다. 연령대에 따라 환자 집단은 성인, 중년, 노인, 소아로 분류되며, 각각 고유한 임상적 우선순위, 순응 행동, 미적 또는 기능적 선호도를 나타내며, 제품 특징과 커뮤니케이션 전략에 반영해야 합니다.

목차

제1장 서문

제2장 조사 방법

제3장 주요 요약

제4장 시장 개요

제5장 시장 인사이트

제6장 미국 관세의 누적 영향 2025

제7장 AI의 누적 영향 2025

제8장 근시 및 노안 치료 시장 : 치료 유형별

  • 백내장 수술
  • 교정 렌즈
    • 콘택트렌즈
    • 안경
    • 다초점 렌즈
    • 각막굴절 교정 렌즈
  • 임플란트 렌즈
  • 외과적 치료

제9장 근시 및 노안 치료 시장 : 연령층별

  • 성인
  • 중년
  • 고령자
  • 소아

제10장 근시 및 노안 치료 시장 : 질환 유형별

  • 근시 치료
  • 노안 치료

제11장 근시 및 노안 치료 시장 : 유통 채널별

  • 오프라인
    • 병원
    • 안경점
    • 전문 클리닉
  • 온라인

제12장 근시 및 노안 치료 시장 : 지역별

  • 아메리카
    • 북미
    • 라틴아메리카
  • 유럽, 중동 및 아프리카
    • 유럽
    • 중동
    • 아프리카
  • 아시아태평양

제13장 근시 및 노안 치료 시장 : 그룹별

  • ASEAN
  • GCC
  • EU
  • BRICS
  • G7
  • NATO

제14장 근시 및 노안 치료 시장 : 국가별

  • 미국
  • 캐나다
  • 멕시코
  • 브라질
  • 영국
  • 독일
  • 프랑스
  • 러시아
  • 이탈리아
  • 스페인
  • 중국
  • 인도
  • 일본
  • 호주
  • 한국

제15장 경쟁 구도

  • 시장 점유율 분석, 2024
  • FPNV 포지셔닝 매트릭스, 2024
  • 경쟁 분석
    • ABB Optical Group
    • AbbVie Inc.
    • AccuLens
    • Alcon Inc.
    • ARCTIC VISION HONG KONG BIOTECH LIMITED
    • Bausch & Lomb Incorporated.
    • Carl Zeiss AG
    • EssilorLuxottica
    • Euclid Systems Corporation
    • Eyenovia, Inc.
    • Haag-Streit Group
    • HOYA Vision Care Europe Hoya Holdings N.V.
    • Johnson & Johnson Vision Care, Inc.
    • LENZ Therapeutics, Inc.
    • Menicon Co., Ltd.
    • NIDEK CO., LTD.
    • Orasis Pharmaceuticals, Ltd
    • Regeneron Pharmaceuticals Inc.
    • SCHWIND eye-tech-solutions GmbH
    • Sydnexis, Inc.
    • The Cooper Companies Inc.
    • Topcon Corporation
    • Ziemer Ophthalmic Systems AG
LSH 25.10.22

The Myopia & Presbyopia Treatment Market is projected to grow by USD 45.77 billion at a CAGR of 9.49% by 2032.

KEY MARKET STATISTICS
Base Year [2024] USD 22.14 billion
Estimated Year [2025] USD 24.13 billion
Forecast Year [2032] USD 45.77 billion
CAGR (%) 9.49%

A strategic overview of converging clinical innovations, demographic pressures, and patient expectations that are reshaping refractive care delivery and commercialization

The landscape of refractive care is undergoing a phase of rapid transformation driven by concurrent clinical innovations, demographic shifts, and evolving patient expectations. Advances in optical devices, surgical techniques, and pharmacologic interventions are reshaping traditional care pathways for both myopia and presbyopia, while changes in care delivery and distribution channels are altering how patients access solutions. Clinicians are adapting to a broader array of therapeutic options and balancing long-standing surgical approaches with emerging noninvasive and pharmacologic tools, which is expanding the range of acceptable care plans and altering referral patterns.

At the same time, patient demand is becoming more nuanced; digital-native cohorts expect convenience and personalized options, and older adults seek solutions that preserve functional vision in everyday tasks. These shifts require manufacturers, service providers, and payers to rethink product design, clinical training, and reimbursement conversations. The interplay between clinical evidence generation and commercial adoption is increasingly important, and stakeholders who can align efficacy data with operational feasibility and patient experience will gain competitive advantage. In short, the introduction sets the stage for a strategic appraisal of clinical, regulatory, and commercial vectors that will determine near-term priorities and longer-term value creation in refractive care.

How convergent clinical breakthroughs, digital engagement, and care pathway reconfiguration are rapidly redefining treatment approaches and market dynamics in refractive healthcare

The past several years have produced transformative shifts across clinical practice, technology, and patient pathways that are redefining care for refractive errors. Clinically, the adoption curve for minimally invasive and lens-based interventions has accelerated as surgical techniques and intraocular lens optics evolve to address presbyopia with improved visual quality and reduced dysphotopsia. Simultaneously, myopia management has graduated from preventive advisories to structured treatment algorithms thanks to broader acceptance of pharmacologic options and behavioral interventions tailored for younger patients. These clinical advances are reshuffling the therapeutic hierarchy and prompting new cross-disciplinary collaborations between ophthalmology, optometry, and primary care.

Commercially, digital channels and direct-to-consumer models have increased patient awareness and demand, forcing traditional distribution and clinical models to adapt. Device manufacturers and service providers are investing in digital tools for remote screening, adherence monitoring, and postoperative care, which are extending the care continuum and changing revenue streams. Regulatory attention on quality of outcomes and long-term safety has increased, accelerating the need for robust real-world evidence. As a result, organizational priorities now include bolstering clinical evidence generation, enhancing digital engagement capabilities, and strengthening supply chain resilience to ensure reliable product access across care settings.

Assessing the practical consequences of trade policy shifts on procurement, supply chains, and strategic sourcing decisions across refractive care stakeholders

Tariff policy changes and trade measures enacted in and around 2025 introduced a fresh set of considerations for supply chains, procurement, and pricing within the refractive care ecosystem. When tariffs increase import costs for surgical instruments, lenses, and ancillary devices, purchasers and manufacturers experience immediate pressure on input costs and procurement timelines. Historically observed responses to such trade shocks include strategic sourcing adjustments, increased inventory buffering, and accelerated supplier diversification, all of which can reshape the distribution networks that support clinics and optical retailers.

More specifically, tariff-driven cost pressures often lead manufacturers to evaluate local assembly or near-shoring for key components to reduce exposure to cross-border duties and to maintain pricing competitiveness. Healthcare providers respond by timing purchases, renegotiating service contracts, and prioritizing products with stable supply chains. Payers and procurement entities may intensify scrutiny of cost-effectiveness and total cost of ownership, prompting device vendors to highlight clinical outcomes and long-term value. Overall, the cumulative impact of tariff-related measures is to incentivize supply chain resilience, contractual flexibility, and greater transparency in cost structures, prompting durable strategic shifts rather than transient adjustments.

Strategically actionable segmentation analysis that aligns treatment modalities, patient demographics, disease categories, and distribution channels to optimize clinical adoption and commercial impact

Insightful segmentation enables stakeholders to tailor product development, clinical trials, and go-to-market strategies to the distinct needs of each cohort and care pathway. Based on treatment type, the field spans cataract surgery, corrective lenses, implantable lenses, and surgical treatments, with corrective lenses further differentiated into contact lenses, eyeglasses, multifocal lenses, and orthokeratology lenses; this diversity points to multiple concurrent innovation pipelines and differentiated commercialization approaches. Based on age group, patient populations are organized into adults, middle-aged, older adults, and pediatric cohorts, each of which exhibits unique clinical priorities, adherence behaviors, and aesthetic or functional preferences that must be reflected in product features and communication strategies.

Based on disease type, the market is defined by myopia treatment and presbyopia treatment, and each condition demands distinct outcome measures, safety profiles, and long-term management plans. Based on distribution channel, care is delivered through offline and online channels, with offline distribution further featuring hospitals, optical stores, and specialty clinics; the coexistence of these channels requires integrated omnichannel strategies that ensure consistent clinical onboarding, follow-up care, and patient education. Together, these complementary segmentation lenses illuminate where investment in clinical evidence, patient support, and channel-specific marketing will have the greatest strategic payoff, and they highlight the necessity of aligning product attributes with the operational realities of each delivery model.

Deep regional perspectives on clinical adoption, regulatory diversity, and distribution models across the Americas, Europe Middle East and Africa, and Asia-Pacific environments

Regional dynamics materially influence regulatory pathways, reimbursement practices, and adoption patterns for refractive solutions. In the Americas, patient demand is shaped by a combination of established surgical infrastructures, high consumer awareness, and growing interest in noninvasive interventions, which together create opportunities for premium optics and integrated care models. Regulatory agencies in the region emphasize evidence of clinical safety and functional outcomes, and payers increasingly focus on total patient experience and productivity gains associated with successful interventions. These factors encourage manufacturers to prioritize robust clinical programs and clinician education initiatives to support adoption.

In Europe, Middle East & Africa, adoption heterogeneity is pronounced; advanced healthcare systems in parts of Europe adopt novel lens technologies and device-driven workflows quickly, while other subregions prioritize scalable, cost-effective solutions that can be deployed through established optical retail and hospital networks. Regulatory diversity across countries requires nuanced market entry strategies and adaptive pricing models. In Asia-Pacific, demographic trends and high prevalence of myopia in younger cohorts create strong demand for both preventive and corrective interventions, while rapid digital adoption supports telehealth-enabled screening and adherence solutions. Supply chain proximity and manufacturing capacity in the region also influence global sourcing strategies and collaborative innovation models.

How integrated innovation strategies, clinician enablement, and outcome-focused commercial models are reshaping competitive positioning among refractive care solution providers

Competitive dynamics in refractive care are characterized by a dual emphasis on differentiated clinical efficacy and integrated lifecycle support that spans preoperative screening through long-term follow-up. Leading organizations are concentrating R&D on optics that deliver superior functional outcomes across lighting conditions, and on platforms that simplify surgical workflows while improving predictability of results. Concurrently, companies that pair product innovation with clinician training programs and outcome-tracking systems strengthen their position by lowering the barrier to adoption for complex interventions.

Partnerships and strategic alliances between device makers, lens manufacturers, and care delivery networks are increasingly common as stakeholders seek to combine clinical expertise with distribution reach. Similarly, investment in digital tools for patient engagement, remote monitoring, and data analytics is becoming table stakes for companies that want to demonstrate real-world performance. Pricing strategies are evolving to reflect outcome-based conversations, and organizations that can present clear evidence of sustained visual function and quality-of-life improvements are better positioned in negotiations with health systems and large group purchasers. Overall, the competitive environment rewards integrated solutions that combine superior optics, clinician enablement, and measurable patient benefit.

Actionable, priority-driven recommendations to synchronize clinical evidence, supply resilience, and omnichannel commercialization for sustainable leadership in refractive care

Industry leaders must move from reactive optimization to proactive strategy by aligning clinical evidence generation, supply chain resilience, and patient-centric commercialization. First, prioritize investment in clinical studies that demonstrate functional vision benefits and long-term safety across diverse patient cohorts, ensuring that evidence generation is structured to inform both regulatory submissions and payer dialogues. Second, diversify sourcing and evaluate near-shoring or multi-supplier models for critical components to mitigate exposure to trade disruptions while maintaining quality control and lead-time reliability. Third, design omnichannel engagement strategies that integrate offline clinical care with online patient education and remote monitoring to enhance adherence and long-term outcomes.

Additionally, focus on clinician enablement through targeted training, outcome-tracking tools, and shared decision-making resources that make it easier for providers to adopt new modalities. Strengthen partnerships with optical retailers and specialty clinics to expand points of care for both screening and follow-up services. Finally, embed value demonstration into commercial discussions by linking clinical outcomes to downstream benefits such as reduced dependency on corrective devices and improved patient productivity, thereby improving the persuasiveness of reimbursement conversations and tender responses.

A robust mixed-methods research approach integrating clinical literature, practitioner interviews, and distribution channel analysis to ground strategic insights in multi-stakeholder realities

The research underpinning this analysis combines systematic literature review, targeted expert interviews, and qualitative synthesis of recent clinical and commercial developments. Peer-reviewed clinical publications and regulatory filings provided the foundation for evaluating the relative maturity and safety profiles of surgical, lens-based, and pharmacologic interventions. These sources were complemented by structured interviews with clinicians across refractive surgery, optometry, and pediatric ophthalmology to capture practice-level insights on adoption drivers, patient preferences, and referral dynamics.

Commercial and distribution perspectives were informed by conversations with supply chain managers, retail operators, and digital health specialists to understand channel performance and logistical constraints. The methodology emphasized triangulation across clinical evidence, practitioner experience, and channel realities to ensure that the analysis reflects multi-stakeholder considerations. Wherever possible, findings were cross-validated against recent public guidance from regulatory bodies and consensus statements from professional societies to maintain alignment with accepted standards of care and to highlight areas where real-world practice is evolving more rapidly than formal guidance.

Concluding synthesis linking clinical innovation, operational execution, and commercial strategy to capture sustained value and improve patient outcomes in refractive care

In sum, the confluence of technological innovation, shifting patient expectations, and changing distribution dynamics is creating both opportunities and complexities for stakeholders involved in myopia and presbyopia care. Clinically, a broader arsenal of interventions means that personalized treatment strategies must account for lifecycle considerations, patient lifestyle, and long-term safety. Commercially, channel evolution and trade dynamics require flexible go-to-market approaches and resilient supply chain architectures. Organizations that successfully bridge clinical proof points with practical implementation support-through clinician training, robust evidence programs, and integrated patient engagement-will secure differentiated adoption pathways.

Moving forward, the imperative is clear: align product innovation with measurable outcomes and operational feasibility, and embed adaptability within commercial and sourcing strategies. By doing so, stakeholders can not only respond to near-term disruptions but also capture the long-term value created by improved visual function and enhanced patient experience. The conclusions emphasize the need for coordinated action across development, regulatory, and commercialization functions to ensure that clinical advances translate into sustainable patient and business benefits.

Table of Contents

1. Preface

  • 1.1. Objectives of the Study
  • 1.2. Market Segmentation & Coverage
  • 1.3. Years Considered for the Study
  • 1.4. Currency & Pricing
  • 1.5. Language
  • 1.6. Stakeholders

2. Research Methodology

3. Executive Summary

4. Market Overview

5. Market Insights

  • 5.1. Rising adoption of low-dose atropine eye drops as first-line myopia control in children
  • 5.2. Increased preference for extended depth of focus intraocular lenses for presbyopia correction in cataract surgeries
  • 5.3. Growing investment in smart contact lens technologies for continuous myopia progression monitoring in adolescents
  • 5.4. Surge in teleophthalmology platforms offering remote myopia management consultations and digital compliance tracking tools
  • 5.5. Expansion of pharmaceutical research pipelines focusing on combined anti-myopia and presbyopia pharmacological therapies
  • 5.6. Integration of 3D printed personalized spectacle lenses for bespoke myopia and presbyopia optical corrections
  • 5.7. Emergence of blue light filtering lens coatings aiming to reduce digital eye strain associated with early presbyopia symptoms
  • 5.8. Strategic partnerships between biotech startups and ophthalmic device manufacturers for innovative presbyopia treatment devices

6. Cumulative Impact of United States Tariffs 2025

7. Cumulative Impact of Artificial Intelligence 2025

8. Myopia & Presbyopia Treatment Market, by Treatment Type

  • 8.1. Cataract Surgery
  • 8.2. Corrective Lenses
    • 8.2.1. Contact Lenses
    • 8.2.2. Eyeglasses
    • 8.2.3. Multifocal Lenses
    • 8.2.4. Orthokeratology Lenses
  • 8.3. Implantable Lenses
  • 8.4. Surgical Treatments

9. Myopia & Presbyopia Treatment Market, by Age Group

  • 9.1. Adults
  • 9.2. Middle-aged
  • 9.3. Older Adults
  • 9.4. Pediatric

10. Myopia & Presbyopia Treatment Market, by Disease Type

  • 10.1. Myopia Treatment
  • 10.2. Presbyopia Treatment

11. Myopia & Presbyopia Treatment Market, by Distribution Channel

  • 11.1. Offline
    • 11.1.1. Hospitals
    • 11.1.2. Optical Stores
    • 11.1.3. Specialty Clinics
  • 11.2. Online

12. Myopia & Presbyopia Treatment 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. Myopia & Presbyopia Treatment Market, by Group

  • 13.1. ASEAN
  • 13.2. GCC
  • 13.3. European Union
  • 13.4. BRICS
  • 13.5. G7
  • 13.6. NATO

14. Myopia & Presbyopia Treatment 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. ABB Optical Group
    • 15.3.2. AbbVie Inc.
    • 15.3.3. AccuLens
    • 15.3.4. Alcon Inc.
    • 15.3.5. ARCTIC VISION HONG KONG BIOTECH LIMITED
    • 15.3.6. Bausch & Lomb Incorporated.
    • 15.3.7. Carl Zeiss AG
    • 15.3.8. EssilorLuxottica
    • 15.3.9. Euclid Systems Corporation
    • 15.3.10. Eyenovia, Inc.
    • 15.3.11. Haag-Streit Group
    • 15.3.12. HOYA Vision Care Europe Hoya Holdings N.V.
    • 15.3.13. Johnson & Johnson Vision Care, Inc.
    • 15.3.14. LENZ Therapeutics, Inc.
    • 15.3.15. Menicon Co., Ltd.
    • 15.3.16. NIDEK CO., LTD.
    • 15.3.17. Orasis Pharmaceuticals, Ltd
    • 15.3.18. Regeneron Pharmaceuticals Inc.
    • 15.3.19. SCHWIND eye-tech-solutions GmbH
    • 15.3.20. Sydnexis, Inc.
    • 15.3.21. The Cooper Companies Inc.
    • 15.3.22. Topcon Corporation
    • 15.3.23. Ziemer Ophthalmic Systems AG
샘플 요청 목록
0 건의 상품을 선택 중
목록 보기
전체삭제