F2 Labs Press Release

Recognition Highlights F2 Labs’ Leadership in Medical Device Testing, FDA Compliance, EMC Testing, Wireless Certification, and Global Market Access Services

F2 Labs, a leading independent medical device testing, compliance, and certification laboratory, today announced it has been recognized as the Top Medical Product Compliance & Certification Testing Lab 2026 by MedTech Business Review. The publication also named F2 Labs among its Top Medical Device Testing Services Providers for 2026.

The recognition underscores F2 Labs’ role in helping medical device manufacturers accelerate product development, reduce regulatory risk, and achieve compliance with U.S., Canadian, European, and international market requirements.

As medical devices become increasingly connected, wireless, and software-enabled, manufacturers face growing challenges related to regulatory compliance, electromagnetic compatibility (EMC), electrical safety, wireless certification, cybersecurity considerations, and global market access. F2 Labs supports organizations throughout the product lifecycle by providing integrated testing, certification, and regulatory guidance designed to streamline approvals and shorten time to market.

According to the MedTech Business Review feature, F2 Labs helps manufacturers address compliance requirements earlier in the development process, enabling design teams to identify potential regulatory issues before they become costly delays.

F2 Labs provides a comprehensive range of medical device testing and certification services, including:

• Medical device EMC and EMI testing
• IEC 60601 electrical safety testing
• Wireless and RF compliance testing
• Environmental and reliability testing
• FDA ASCA-accredited laboratory services
• FDA 510(k) testing support
• NRTL certification programs
• CE Marking support for European market access
• SCC certification requirements for Canada
• International regulatory approvals and global market access services

“Medical device manufacturers are under increasing pressure to bring innovative products to market while meeting complex regulatory and compliance requirements,” said Wendy Fuster, President of F2 Labs. “We are honored to be recognized by MedTech Business Review for our commitment to helping clients navigate testing, certification, and regulatory pathways with technical expertise, responsive service, and practical guidance.”

The feature was developed by the MedTech Business Review editorial and research team following an interview with Wendy Fuster regarding industry trends, evolving compliance challenges, and F2 Labs’ approach to supporting medical technology innovators.

Organizations developing medical devices, connected healthcare technologies, diagnostic equipment, wearable medical products, and other regulated healthcare technologies rely on F2 Labs for testing and certification services that support regulatory compliance, product safety, and successful market entry.

The full feature is available at:
https://www.medtechbusinessreview.com/f2-labs-2026

About F2 Labs

F2 Labs is an independent testing, inspection, certification, and regulatory compliance laboratory serving medical device manufacturers and technology companies throughout North America and global markets. The company provides EMC testing, EMI testing, wireless certification, electrical safety testing, environmental testing, product compliance evaluations, FDA support services, CE Marking assistance, and market access solutions for regulated products.

With more than 30 years of industry experience and laboratory facilities in Maryland, Ohio, and Indiana, F2 Labs helps organizations achieve compliance efficiently while reducing certification timelines and regulatory risk. The company is recognized for its technical expertise, responsive customer service, and comprehensive approach to product testing and certification.

Learn more at www.f2labs.com

Media Contact

Tom Jackson
Marketing & Business Development Specialist
F2 Labs
tjackson@f2labs.com
(240) 782-1745
https://f2labs.com