Preparing Your Medical Device NewCo For IP Due Diligence

IRVINE, Calif., July 22, 2026 – Leading intellectual property law firm Knobbe Martens is proud to share that the firm and several of its partners are shortlisted in eight categories...

The U.S. Food and Drug Administration (FDA) has increasingly emphasized the use of real-world evidence (RWE) to support regulatory decision-making for medical devices. As medical technologies evolve and data sources...

On June 5, 2026, the U.S. Food and Drug Administration (FDA) issued updated guidance stating its intent to exempt certain unclassified medical devices from premarket 510(k) requirements, and that the FDA believes the identified device...