Medical Device Testing And Certification - Market Share Analysis, Industry Trends & Statistics, Growth Forecasts (2026 - 2031)

According to Mordor Intelligence, the medical device testing and certification market size was valued at USD 10.55 billion in 2025 and estimated to grow from USD 10.95 billion in 2026 to reach USD 13.15 billion by 2031, at a CAGR of 3.75% during the forecast period (2026-2031).

This report Segments the Industry Into by Service Type (Testing Services, Inspection Services and More), by Device Class (Class I, Class II, and More), by Testing Type (Biocompatibility Testing, Sterility & Microbiology Testing and More), and by Geography (North America, Europe and More). The Market Forecasts are Provided in Terms of Value (USD).

Global Medical Device Testing And Certification Market Trends and Insights

Regulatory tightening under EU MDR and FDA Safer Devices Act

The 2024-2028 MDR transition window obliges every legacy device to re-seek CE marking under 23 General Safety and Performance Requirements, tripling technical-file depth for many manufacturers ec.europa.eu. Concurrently, Section 524B of the Safer Devices Act mandates U.S. pre-market submissions that include Software Bills of Materials and vulnerability management plans, expanding documentation for every connected product. The combined effect triggered a 40% surge in notified-body applications and elongated average review times beyond 24 months, prompting firms to outsource larger validation packages to accredited laboratories.

Rise in AI/ML-enabled devices driving specialized validation needs

The FDA's public database recorded 882 cleared AI/ML medical devices by May 2024, up 45% year-on-year. Each algorithm demands bias detection, dataset shift analysis, and real-world performance monitoring, tests that exceed classical verification. The EU AI Act, classifying medical AI as "high risk", further requires lifecycle risk management. Laboratories offering algorithm audit services therefore command premium pricing, and this service line is forecast to become a core revenue pillar of the medical device testing & certification services market over the coming decade.

Limited capacity & long lead times at notified bodies

Only 43 notified bodies serve the entire EU under MDR, and application-to-certification ratios exceed 4:1. Average review times rose from 14 months in 2022 to more than 26 months by late-2024. Manufacturers have consequently withdrawn certain low-margin products from the EU, shrinking potential testing volumes and tempering growth in the medical device testing & certification services market.

Other drivers and restraints analyzed in the detailed report include:

1. Growth of home & wearable diagnostics expanding test volumes
2. Mandatory cybersecurity pre-market submissions
3. High testing costs for SMEs & start-ups

For complete list of drivers and restraints, kindly check the Table Of Contents.

Segment Analysis

Testing services held 55.98% of medical device testing & certification market share in 2025, reflecting their status as the unavoidable regulatory entry ticket for all device classes. Certification services track behind because only EU and UK routes legally require third-party auditing, whereas the U.S. relies more on manufacturer self-attestation. However, as regulators intensify post-market surveillance, inspection & auditing revenues are gaining momentum.

Cybersecurity and software validation-still statistically nested within testing services-represent the fastest revenue stream, posting 5.03% CAGR on account of the FDA and Health Canada mandates. Laboratories that integrate biological, mechanical, and digital-security benches in one location cut total turn-around time by up to 30%, enabling premium billing and reinforcing competitive moat. Consequently, the medical device testing & certification market is shifting toward bundled, subscription-like quality-assurance contracts that lock in multi-year revenue visibility.

Continued investments in automated sample preparation and high-throughput analytics have trimmed direct labor per report by nearly 10% since 2022, raising operating margins. Certification services, hampered by notified-body scarcity, are forecast to grow at a slower 2.44% but remain indispensable for EU market access, sustaining a defensive revenue floor.

Complete Report Scope:

• By Service Type
  • Testing Services
  • Certification Services
  • Inspection & Auditing Services
  • Others
• By Device Class
  • Class I
  • Class II
  • Class III
  • In Vitro Diagnostic Devices
• By Testing Type
  • Biocompatibility Testing
  • Sterility & Microbiology Testing
  • Electrical Safety & EMC
  • Software & Cybersecurity Testing
  • Mechanical & Physical Testing
  • Packaging & Shelf-life Testing
• By Geography
  • North America
    • United States
    • Canada
    • Mexico
  • Europe
    • Germany
    • United Kingdom
    • France
    • Italy
    • Spain
    • Rest of Europe
  • Asia-Pacific
    • China
    • India
    • Japan
    • South Korea
    • Australia
    • Rest of Asia-Pacific
  • South America
    • Brazil
    • Argentina
    • Rest of South America
  • Middle East and Africa
    • GCC
    • South Africa
    • Rest of Middle East and Africa

Geography Analysis

North America captured 38.42% of the medical device testing & certification services market in 2025, anchored by the FDA's streamlined 510(k) and Breakthrough Device pathways that catalyze continuous product launches. Domestic laboratories benefit from deep payer systems that fund innovation and from a regulatory environment that explicitly recognizes several voluntary consensus standards, shortening validation cycles. From 2026-2031, the region is set to expand at 3.05% CAGR, slower than the global mean due to maturity.

Asia-Pacific is the clear volume engine, forecast to grow 6.42% annually. China's updated Medical Device Regulation, effective July 2024, compels local producers to secure third-party biocompatibility and packaging data, driving steady sample inflows to regional labs. India's Medical Device Rules amendment of 2024 extended third-party audit requirements to additional product categories, adding incremental demand. Foreign players are rapidly opening satellite laboratories in Suzhou, Bangalore, and Kuala Lumpur to capture the rising tide.

Europe suffered near-term drag from notified-body scarcity; however, once capacity normalizes, deferred applications will convert to billable tests, helping the region regain momentum beyond 2027. Latin America and the Middle East & Africa remain nascent but benefit from harmonization initiatives, which require proof of compliance with reference-market standards-typically executed by global lab networks.

1. SGS
2. Intertek Group
3. TUV SUD
4. UL Solutions
5. Eurofins
6. BSI Group
7. TUV Rheinland
8. TUV Nord
9. Dekra SE
10. Bureau Veritas
11. DNV GL
12. Nemko
13. NSF International
14. Nelson Labs
15. Element Materials Technology
16. Charles River
17. Smithers
18. Pace Analytical Services
19. Merieux NutriSciences
20. Medistri

Additional Benefits:

• The market estimate (ME) sheet in Excel format
• 3 months of analyst support