시장보고서
상품코드
1870143

두개 천공기 시장 : 종류별, 최종사용자별, 유통 경로별, 용도별, 멸균 방법별 - 세계 예측(2025-2032년)

Cranial Perforators Market by Type, End User, Distribution Channel, Application, Sterilization Method - Global Forecast 2025-2032

발행일: | 리서치사: 360iResearch | 페이지 정보: 영문 181 Pages | 배송안내 : 1-2일 (영업일 기준)

    
    
    




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

두개 천공기 시장은 2032년까지 CAGR 6.84%로 1억 8,724만 달러 규모로 성장할 것으로 예측됩니다.

주요 시장 통계
기준 연도 2024년 1억 1,023만 달러
추정 연도 2025년 1억 1,772만 달러
예측 연도 2032 1억 8,724만 달러
CAGR(%) 6.84%

두개골 천공 가지를 형성하는 장치, 임상, 조달 동향 및 이해관계자의 전략적 우선순위에 대한 간략한 주요 요약

본 Executive Summary는 두개골 천공술의 현황에 대한 간결하고 실질적인 입문서로서, 기기 선택과 도입을 재구성하고 있는 임상적, 상업적, 운영상의 진전을 통합하여 제공합니다. 목표는 기술 선택의 기초가 되는 미묘한 증거 기반을 유지하면서 제조업체, 병원 조달팀, 유통업체, 임상 챔피언에게 중요한 핵심 동향을 정리하는 것입니다.

임상적 기대, 디바이스 엔지니어링의 발전, 공급망 재구축의 수렴으로 두개골 천공술에서 조달과 혁신이 공동으로 재정의되는 방식

두개골 천공기의 환경은 기술적 정교화, 임상적 선호도 변화, 의료 제공 시스템 내 인프라 압력에 의해 추진되는 일련의 변혁적 변화를 경험하고 있습니다. 파워트레인 설계의 발전으로 토크의 일관성, 저진동 특성, 모듈식 헤드 구성에 중점을 둔 선택지가 생겨나면서 외과의사는 사례의 복잡성과 해부학적 제약에 가장 적합한 기기를 선택할 수 있게 되었습니다. 동시에, 내비게이션 호환성 및 통합 안전 연동과 같은 보조 기술의 채택은 수술 중 위험을 줄이고 정확도를 향상시키는 데 중점을 둔 임상의의 태도를 반영합니다.

관세로 인한 비용 변동 이후 조달-재고-유통 전략 재구축 : 공급업체 다변화 및 니어쇼어링 검토 가속화

2025년 미국의 관세 조정으로 인해 새로운 투입 비용이 발생하여 두개골 천공기에 사용되는 장비 및 부품 조달, 재고 계획, 가격 전략에 영향을 미쳤습니다. 모터, 정밀 주조품, 전자 제어 모듈을 국경을 초월한 공급망에 의존하던 제조업체들은 비용 흡수, 다운스트림 전가, 또는 조달 방식 재설계를 통한 리스크 감소 등 개별적인 판단을 내려야 했습니다. 일부 기업들은 즉각적인 영향으로 공급업체 다변화가 가속화되고, 리드타임 안정화와 착륙 비용의 변동성을 억제하기 위해 니어쇼어링 기회를 적극적으로 검토하고 있습니다.

심층 세분화 분석을 통해 기기 유형, 임상 환경, 유통 경로, 외과적 적용, 멸균 호환성이 각기 다른 도입 경로를 주도하는 방식을 파악할 수 있었습니다.

세분화를 통해 유형, 최종사용자, 유통 채널, 용도, 멸균 방법별로 서로 다른 가치 동인과 채택 경로를 파악할 수 있습니다. 장치 유형을 고려하면, 휴대성과 배터리 구동 시간이 하이브리드 수술실의 배선 관련 문제를 줄여주는 배터리 구동 솔루션이 선호되는 반면, 지속적인 고토크 애플리케이션의 경우 지속적인 전원 공급이 가능한 유선 전기식이 여전히 선호되고 있습니다. 또한, 단순하고 멸균 가능한 메커니즘과 확립된 유지보수 절차가 우선시되는 환경에서는 공압식 시스템이 계속 선택되고 있습니다. 최종사용자의 특성은 조달 및 사용 패턴에 영향을 미칩니다 : 외래 수술 센터에서는 처리 시간과 기기의 휴대성을 중요시하는 경향이 있습니다. 병원에서는 입원 및 외래 시설을 넘나들며 기기 평가가 이루어지며, 비교육병원과 교육병원은 수련체계와 사례의 복잡성 차이가 사양에 영향을 미칩니다. 전문 클리닉에서는 시술에 특화된 인체공학적 설계와 비용 효율성이 우선시됩니다.

채용 및 상용화 전략 수립, 아메리카, 유럽, 중동 및 아프리카, 아시아태평양의 지역 간 차이 및 조달 트렌드

지역별 동향은 규제 요건, 구매 행동, 임상 도입 패턴에 중요한 영향을 미칩니다. 미국 대륙에서는 주요 병원 시스템 및 구매 컨소시엄에 의한 중앙 집중식 조달이 진행되고 있으며, 서비스 수준 계약, 교육, 장기 파트너십에 대한 협상이 활발히 진행되고 있습니다. 이 지역의 임상 현장에서는 디지털 수술실 환경과의 통합성과 다양한 시술에 대응할 수 있는 고기능성 솔루션을 선호합니다. 규제의 명확성과 강력한 시판 후 조사 체계는 새로운 기기의 수용 곡선을 더욱 형성할 것입니다.

기존 제조업체와 모듈성, 임상적 증거 및 서비스 품질을 중시하는 혁신 기업의 경쟁적 행동 및 전략적 전개

경쟁 환경은 기존 의료기기 기업, 전문 의료기기 혁신 기업, 지역 기업이 서비스, 기능적 차별화, 임상적 증거로 경쟁하는 복합적인 구조로 정의됩니다. 주요 제조업체들은 제품 차별화를 위해 모듈성, 인체공학적 개선, 통합 안전 메커니즘에 대한 투자를 진행하는 한편, 도입 리스크를 줄이기 위해 교육 및 유지보수 프로그램 확대에 주력하고 있습니다. 소규모 혁신 기업은 교육 병원 및 전문 클리닉의 초기 도입자에게 어필할 수 있는 조용한 모터, 빠른 헤드 교체, 혁신적인 클러치 시스템과 같은 틈새 성능 우위에 초점을 맞추는 경향이 있습니다.

제조업체 및 유통업체를 위한 제품 개발, 증거 창출, 공급망 탄력성을 고객의 요구에 부합하도록 하기 위한 실행 가능한 전략적 우선 순위

리더는 제품 로드맵과 상업적 모델을 임상의, 멸균 팀, 조달 담당자의 수렴된 요구에 맞게 조정해야 합니다. 모듈식 헤드 옵션과 성인 및 소아 뇌신경 수술 워크플로우에 적합한 인체공학적 설계를 갖춘 장치 개발을 우선시하고, 여러 멸균 방법과의 기본 호환성을 보장하여 의료기관의 유연성을 극대화합니다. 안전성, 조작성, 수술 시작까지의 시간 등의 지표를 정량화하는 표적화된 레지스트리 및 외과의사 주도의 전향적 연구에 투자하여 임상적 증거 창출을 강화하십시오. 이를 통해 도입 주기를 단축하고 지불자의 증거 요구 사항을 충족할 수 있습니다.

의료진 인터뷰, 기술 사양 분석, 공급망 매핑을 결합한 강력한 혼합 방법론 조사를 통해 의료기기 및 상업적 지식을 검증합니다.

본 조사에서는 1차 인터뷰, 2차 문헌 통합, 장비 사양 분석, 공급망 매핑을 결합한 혼합 방법을 사용했습니다. 1차 데이터에는 신경외과, 구강외과, 정형외과 임상 리더, 병원, 외래 수술 센터, 전문 클리닉의 조달 책임자, 유통 및 서비스 관리자와의 구조화된 대화를 통해 운영 실태를 파악했습니다. 이러한 논의는 실제 의사결정 기준, 멸균 방법, 시판 후 서비스에 대한 기대치를 명확히 하는 것을 목적으로 합니다.

임상적 요인, 상업적 요인, 공급망 요인을 통합하여 증거, 서비스, 조달 방법이 두개골 천공기 분야의 장기적인 리더십을 결정하는 메커니즘을 보여줍니다.

두개골 천공기 생태계는 전환점에 있으며, 임상적 요구, 기기 설계, 상업적 모델이 일치하여 채택 기준과 경쟁 우위를 재정의하고 있습니다. 임상의는 정확성과 안전성을 우선시하고, 조달팀은 멸균 대응이 가능하고 유지보수가 용이하며 처리 능력을 최적화할 수 있는 솔루션을 원하며, 유통업체는 규모와 지역 대응력의 균형 잡힌 모델을 추구하고 있습니다. 무역의 변화는 유연한 조달과 비상 계획의 중요성을 강조하고, 지역적 차이는 개별 대응 전략의 필요성을 보여줍니다.

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 두개 천공기 시장 : 유형별

  • 배터리 구동식
  • 코드식 전기식
  • 공기압식

제9장 두개 천공기 시장 : 최종사용자별

  • 외래 수술 센터
  • 병원
    • 비교육 병원
    • 교육 병원
  • 전문 클리닉

제10장 두개 천공기 시장 : 유통 채널별

  • 직접 판매
  • 판매대리점
    • 지역 판매대리점
    • 전국 판매대리점
  • 온라인 판매

제11장 두개 천공기 시장 : 용도별

  • 신경외과
    • 성인 신경외과
    • 소아 신경외과
  • 구강외과
  • 정형외과 수술

제12장 두개 천공기 시장 멸균 방법별

  • 저온 멸균
  • 방사선 멸균
  • 증기 멸균

제13장 두개 천공기 시장 : 지역별

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

제14장 두개 천공기 시장 : 그룹별

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

제15장 두개 천공기 시장 : 국가별

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

제16장 경쟁 구도

  • 시장 점유율 분석, 2024
  • FPNV 포지셔닝 매트릭스, 2024
  • 경쟁 분석
    • Medtronic plc
    • Stryker Corporation
    • Zimmer Biomet Holdings, Inc.
    • B. Braun Melsungen AG
    • Johnson & Johnson
    • Integra LifeSciences Holdings Corporation
    • KLS Martin Group
    • Medartis AG
    • De Soutter Medical Limited
    • Sklar Instruments Inc.
KSM 25.12.01

The Cranial Perforators Market is projected to grow by USD 187.24 million at a CAGR of 6.84% by 2032.

KEY MARKET STATISTICS
Base Year [2024] USD 110.23 million
Estimated Year [2025] USD 117.72 million
Forecast Year [2032] USD 187.24 million
CAGR (%) 6.84%

Concise executive framing of device, clinical, and procurement dynamics shaping cranial perforators and the strategic priorities for stakeholders

This executive summary delivers a concise yet substantive primer on the cranial perforators landscape, synthesizing clinical, commercial, and operational developments that are reshaping device selection and adoption. The objective is to frame the core dynamics that matter to manufacturers, hospital procurement teams, distributors, and clinical champions, while preserving the nuanced evidence base that underpins technology choices.

Clinicians increasingly demand devices that combine precision, ergonomic control, and compatibility with contemporary sterilization workflows. Simultaneously, providers and distributors are navigating procurement pressures that prioritize uptime, staff safety, and long-term value. These intersecting pressures are driving investment in product features, clinical training, and supply chain reliability. From a regulatory and reimbursement perspective, approvals and pathway clarity remain essential for market entry and continued adoption, particularly where pediatric and adult neurosurgical use cases present differentiated clinical risk profiles.

The remainder of the report explores the transformative forces influencing design and distribution, the cascading effects of recent tariff changes, segmentation-specific performance drivers, regional nuances, competitive behaviors, and clear recommendations for leaders seeking to convert insight into action.

How converging clinical expectations, device engineering advances, and supply chain restructuring are jointly redefining procurement and innovation in cranial perforators

The cranial perforators landscape is undergoing a set of transformative shifts driven by technological refinement, clinical preference evolution, and infrastructural pressures within care delivery systems. Advances in powertrain designs have produced options that emphasize torque consistency, lower vibration profiles, and modular head configurations, allowing surgeons to choose the instrument that best matches case complexity and anatomical constraints. Concurrently, the adoption of adjunctive technologies such as navigation compatibility and integrated safety interlocks reflects a broader clinician emphasis on reducing intraoperative risk and improving precision.

On the operational side, hospitals and ambulatory centers are rationalizing device fleets to simplify sterilization workflows and reduce total cost of ownership. This has elevated interest in systems that tolerate multiple sterilization modalities and enable rapid turnaround between cases. Distribution and commercial models are also shifting; direct engagement with large health systems coexists with hybrid approaches that leverage both national distributors for scale and local partners for urgency and service. Finally, stakeholder expectations around clinical evidence and post-market surveillance have risen, prompting manufacturers to invest in training programs, registries, and prospective studies to demonstrate relative safety and ease of use. These combined shifts are redefining procurement criteria, channel economics, and innovation priorities across the ecosystem.

Realignment of sourcing, inventory and distribution strategies after tariff-driven cost shifts that intensified supplier diversification and nearshoring considerations

In 2025, tariff adjustments in the United States introduced new input costs that reverberated across sourcing, inventory planning, and pricing strategies for devices and components used in cranial perforators. Manufacturers that relied on cross-border supply chains for motors, precision castings, and electronic control modules faced discrete decisions about absorbing costs, passing them downstream, or redesigning sourcing to mitigate exposure. For some, the immediate impact was an acceleration of supplier diversification and an active review of nearshoring opportunities to stabilize lead times and control landed cost volatility.

Health systems responded by tightening demand forecasting and lengthening procurement review cycles; this cautious stance prompted some suppliers to increase stock-keeping at regional distribution nodes to preserve service levels. Distributors re-evaluated their contractual terms and service agreements to reflect changed freight and duty profiles, often emphasizing contingency capabilities such as expedited stocking and local repair services. Over time, these adjustments stimulated strategic conversations around product portfolio rationalization, with stakeholders prioritizing devices that combined cross-case versatility with compatibility across sterilization platforms to limit SKU proliferation and reduce tariff-related supply chain fragility.

Deep segmentation analysis exposing how device types, clinical settings, channels, surgical applications, and sterilization compatibility drive distinct adoption pathways

Segmentation reveals differentiated value drivers and adoption pathways across types, end users, distribution channels, applications, and sterilization methods. When device type is considered, Battery Powered solutions appeal where portability and battery autonomy reduce cord-related clutter in hybrid OR setups, while Corded Electric variants remain preferred for sustained high-torque applications due to continuous power delivery, and Pneumatic systems are still selected in environments that prioritize simple, sterilizable mechanics and established maintenance protocols. End user distinctions matter in procurement and utilization patterns: Ambulatory Surgical Centers often emphasize turnaround time and device portability; Hospitals evaluate devices across inpatient and outpatient suites and differentiate needs between Non Teaching Hospitals and Teaching Hospitals, where training and varied case complexity influence specifications; Specialty Clinics prioritize procedure-specific ergonomics and cost-effectiveness.

Distribution channel dynamics shape commercial engagement and service expectations. Direct Sales relationships enable deep integration with large hospital systems through bundled service commitments, whereas Distributors provide breadth and local responsiveness with National Distributors offering scale and Local Distributors delivering on-the-ground support; Online Sales complement these channels by enabling easier access for smaller facilities and streamlined reorder processes. Application-based segmentation shows distinct clinical requirements: Neurosurgery use cases, split between Adult Neurosurgery and Pediatric Neurosurgery, demand the highest precision and smallest footprint designs, Oral Surgery emphasizes access and compact form factors, and Orthopedic Surgery requires robustness for thicker cortical crossings. Sterilization compatibility is a decisive factor for procurement teams; devices that withstand Low Temperature Sterilization, Radiation Sterilization, and Steam Sterilization provide greater institutional flexibility and reduce workflow friction, thereby increasing appeal across end users and distribution models.

Regional contrasts and procurement dynamics across the Americas, Europe Middle East & Africa, and Asia-Pacific that shape adoption and commercialization strategies

Regional dynamics influence regulatory expectations, purchasing behaviors, and clinical adoption patterns in meaningful ways. In the Americas, procurement tends to be centralized within major hospital systems and purchasing consortia, driving negotiations around service level agreements, training, and long-term partnerships. Clinical preference in this region often favors high-feature solutions that integrate with digital OR environments and support extensive procedural variability. Regulatory clarity and robust post-market surveillance frameworks further shape the acceptance curve for new device iterations.

In Europe, Middle East & Africa, heterogeneity among regulatory regimes and hospital procurement models creates variable adoption timelines. Large urban centers and academic hospitals frequently adopt advanced configurations early, while peripheral healthcare providers prioritize cost-efficiency and sterilization compatibility. Distribution networks in this region balance between multinational distributors and local partners who navigate cross-border logistics and compliance requirements.

In Asia-Pacific, growth is driven by expanding surgical capacity, rising investment in infrastructure, and a strong emphasis on cost-competitive solutions that do not sacrifice clinical performance. Local manufacturing capabilities and government procurement programs influence sourcing strategies, while clinicians increasingly demand devices that support both adult and pediatric neurosurgical workflows. Across all regions, service and training offerings are decisive factors for adoption, with regional differences in contracting practices shaping how manufacturers and distributors prioritize investments.

Competitive behaviors and strategic moves across established manufacturers and innovators emphasizing modularity, clinical evidence, and service excellence

Competitive dynamics are defined by a mixture of established medtech firms, specialized device innovators, and regional players that compete on service, feature differentiation, and clinical evidence. Leading manufacturers are investing in modularity, ergonomic improvements, and integrated safety mechanisms to differentiate product offerings while also expanding training and maintenance programs to reduce perceived adoption risk. Smaller innovators tend to focus on niche performance advantages-such as quieter motors, rapid head interchangeability, or novel clutch systems-that appeal to early adopters within teaching hospitals and specialty clinics.

Distribution and after-sales service are important competitive battlegrounds. Companies that provide fast local repair, comprehensive sterilization compatibility guidance, and hands-on surgeon training secure stronger relationships with purchasing teams. Strategic partnerships between device firms and national distributors can accelerate market penetration by leveraging established logistics and service networks, whereas direct-sales models allow suppliers to bundle value-added services and tailor contracts to large integrated delivery networks. Across the competitive set, intellectual property around cutting-head geometries and ergonomic design, combined with clinical evidence generated through registries and prospective studies, continues to be a key differentiator that influences procurement and surgeon preference.

Actionable strategic priorities for manufacturers and distributors to align product development, evidence generation, and supply chain resilience with customer imperatives

Leaders should align product roadmaps and commercial models to the convergent needs of clinicians, sterilization teams, and procurement officers. Prioritize development of devices that offer modular head options and ergonomic designs suited to both adult and pediatric neurosurgical workflows, while ensuring core compatibility with multiple sterilization methods to maximize institutional flexibility. Strengthen clinical evidence generation by investing in targeted registries and surgeon-led prospective studies that quantify safety, ease of use, and time-to-case metrics; this will shorten adoption cycles and support payers' evidentiary requirements.

On the supply side, accelerate supplier diversification and evaluate nearshoring opportunities for critical components to reduce exposure to tariff volatility and freight disruptions. Enhance distributor engagement strategies by offering tiered service packages that provide rapid local repair and training modules for both large health systems and smaller ambulatory centers. Commercial teams should tailor channel strategies to the customer segment: use direct-sales approaches for integrated delivery networks and hybrid distributor partnerships to reach regional and specialty clinic markets. Finally, incorporate scenario planning into price and inventory models to maintain service levels under shifting trade conditions and to protect margins while preserving competitive positioning.

Robust mixed-methods research combining clinician interviews, technical specification analysis, and supply chain mapping to validate device and commercial insights

The research employed a mixed-methods approach combining primary interviews, secondary literature synthesis, device specification analysis, and supply chain mapping. Primary inputs included structured conversations with clinical leaders from neurosurgery, oral surgery, and orthopedic specialties, procurement executives across hospitals, ambulatory surgical centers, and specialty clinics, as well as distribution and service managers to capture operational realities. These discussions were designed to surface real-world decision criteria, sterilization practices, and post-market service expectations.

Secondary research drew from regulatory filings, peer-reviewed clinical studies, device manuals, and publicly available procurement frameworks to validate feature-level claims and sterilization compatibilities. Device technical specifications were analyzed to compare power sources, ergonomic attributes, and compatibility with low temperature, radiation, and steam sterilization methods. Supply chain mapping incorporated import/export flow data, tariff schedules, and distributor footprints to understand how logistics and duties impact landed cost and service responsiveness. Findings were triangulated across data streams to ensure robustness and reviewed by technical advisors with clinical and procurement expertise to confirm practical relevance.

Synthesis of clinical, commercial, and supply chain forces indicating how evidence, service, and sourcing will determine long-term leadership in cranial perforators

The cranial perforators ecosystem is at an inflection point where clinical needs, device engineering, and commercial models are aligning to redefine adoption criteria and competitive advantage. Clinicians prioritize precision and safety, procurement teams seek sterilization-compatible, serviceable solutions that optimize throughput, and distributors press for models that balance scale with local responsiveness. Trade shifts have underscored the importance of flexible sourcing and contingency planning, while regional differences highlight the necessity of tailored engagement strategies.

Moving forward, manufacturers that couple meaningful product differentiation with demonstrable clinical evidence and resilient distribution strategies will be best positioned to capture durable relationships with health systems and specialty providers. Equally, distributors that invest in training, rapid repair capabilities, and hybrid channel models that combine national scale with local service will play a pivotal role in determining which technologies gain traction. Taken together, these factors point to a market where technical performance, service delivery, and supply chain foresight will determine long-term success.

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 ultrasonic bone cutting technology in neurosurgical perforators
  • 5.2. Growing demand for battery-powered cranial perforators with enhanced portability and safety features
  • 5.3. Integration of smart sensor feedback in cranial perforators for real-time surgical guidance and risk reduction
  • 5.4. Expansion of minimally invasive neurosurgery procedures driving demand for precision perforator devices
  • 5.5. Increasing use of 3D-printed customized skull perforator attachments for patient-specific surgical planning
  • 5.6. Emerging collaborations between device manufacturers and academic centers for advanced cranial perforator R&D

6. Cumulative Impact of United States Tariffs 2025

7. Cumulative Impact of Artificial Intelligence 2025

8. Cranial Perforators Market, by Type

  • 8.1. Battery Powered
  • 8.2. Corded Electric
  • 8.3. Pneumatic

9. Cranial Perforators Market, by End User

  • 9.1. Ambulatory Surgical Centers
  • 9.2. Hospitals
    • 9.2.1. Non Teaching Hospitals
    • 9.2.2. Teaching Hospitals
  • 9.3. Specialty Clinics

10. Cranial Perforators Market, by Distribution Channel

  • 10.1. Direct Sales
  • 10.2. Distributors
    • 10.2.1. Local Distributors
    • 10.2.2. National Distributors
  • 10.3. Online Sales

11. Cranial Perforators Market, by Application

  • 11.1. Neurosurgery
    • 11.1.1. Adult Neurosurgery
    • 11.1.2. Pediatric Neurosurgery
  • 11.2. Oral Surgery
  • 11.3. Orthopedic Surgery

12. Cranial Perforators Market, by Sterilization Method

  • 12.1. Low Temperature Sterilization
  • 12.2. Radiation Sterilization
  • 12.3. Steam Sterilization

13. Cranial Perforators 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. Cranial Perforators Market, by Group

  • 14.1. ASEAN
  • 14.2. GCC
  • 14.3. European Union
  • 14.4. BRICS
  • 14.5. G7
  • 14.6. NATO

15. Cranial Perforators 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. Medtronic plc
    • 16.3.2. Stryker Corporation
    • 16.3.3. Zimmer Biomet Holdings, Inc.
    • 16.3.4. B. Braun Melsungen AG
    • 16.3.5. Johnson & Johnson
    • 16.3.6. Integra LifeSciences Holdings Corporation
    • 16.3.7. KLS Martin Group
    • 16.3.8. Medartis AG
    • 16.3.9. De Soutter Medical Limited
    • 16.3.10. Sklar Instruments Inc.
샘플 요청 목록
0 건의 상품을 선택 중
목록 보기
전체삭제