F2 Labs has been named Top Medical Product Compliance & Certification Testing Lab 2026 by MedTech Business Review. The publication also included F2 Labs among its Top Medical Device Testing Services Providers for 2026. (read more)

In March 2026, the Federal Communications Commission (FCC) expanded its "Covered List" to include all foreign-manufactured consumer-grade interet routers, citing national security concerns. This decision prohibits new models of wireless routers from receiving authorization for sale or import in the United States. Devices already on the market or in consumers' homes are not affected. (read more)

EMC testing is often treated as a final compliance checkbox before submitting a 510(k). In reality, it is one of the most common sources of preventable review delays. (read more)

An Industry Insider's Take on FDA General Wellness Policy (read more)

Need help navigating Prop 65 compliance for California? F2 Labs can assist with a Prop 65 evaluation and, in almost all cases, we get through it without testing. (read more)

The FDA has dropped another massive rulebook titled, "Artificial Intelligence-Enabled Device Software Functions: Lifecycle Management and Marketing Submission Recommendations.” Learn more. (read more)

Does customs really check for RoHS in the EU? The answer is yes. This article discusses a few products stopped for RoHS non-compliance. (read more)

“My machine is industrial machinery, do I have to comply with RoHS for CE marking?” We are frequently asked this question. The answer is – yes, unless you fall into one of the exclusions available from the RoHS Directive 2011/65/EU. Read this article to learn more. (read more)

If electrical products had passports, the CE mark would be their golden ticket to travel freely across Europe. But unlike that dusty old passport you forgot to renew, CE marking isn’t just a stamp—it’s a declaration of compliance with essential EU regulations. (read more)

Unregulated Certificates Warning and The Implications Under EU Law (read more)

Do you have a new product and you want to know how it performs before putting it through the rigors of full compliance testing? Contact F2 Labs for help. This is what we do. (read more)

So, you’ve just had the pleasure of hearing from an Authority Having Jurisdiction (AHJ) or an electrical inspector, and their message was something along the lines of: “You’ve failed your inspection!” or “Your equipment needs a ‘UL or CSA Certification!’” Or maybe they dropped the “UL/CSA Certified” or “UL/CSA Labeled (read more)

As we enter an exciting era of technological advancement, the role of artificial intelligence (AI) in medical devices stands out as particularly transformative. The FDA’s recent guidance on “Good Machine Learning Practice” is a crucial milestone in steering this innovation, ensuring that the benefits of AI are realized alongside necessary safeguards. (read more)

F2 Labs can assist you in determining what EMC and Electrical Safety standards and collateral standards are required for certifying your product. (read more)

F2 Labs can assist you in identifying the requirements for CE certification. We have a staff of experts experienced in the CE mark who are ready to assist you throughout the process of CE testing and CE certification. With more than 20 years of experience in CE testing and evaluation, F2 Labs has helped many businesses successfully enter into the European and global markets with CE certi... (read more)

The FDA has been requiring Immunity testing to Common EM emitters and 5G cellular. (read more)