Harness the power of our FDA regulatory experience and expert research and analytical skills.
Our research and analysis could be the foundation for your next multi-million-dollar verdict!
While other firms are fighting over known cases, we're identifying the next generation of mass tort opportunities—hidden in plain sight within FDA databases, adverse event reports, and regulatory filings.
We identify devices with thousands of unreported or misclassified adverse events—ready-made mass tort & MDL cases with minimal competition and massive damages.
We trace single defective devices across dozens or hundreds of relabeled products, revealing cases exponentially larger than anyone realized.
Our proprietary analysis techniques detect patterns of harm buried in FDA data that standard searches miss entirely—giving you first-mover advantage.
We identify falsified premarket data, regulatory violations, and systematic fraud that forms the basis for False Claims Act cases worth billions.
From case identification to courtroom victory, we provide the evidence and expertise you need at every stage.
We identify opportunities others miss through comprehensive regulatory analysis and advanced data mining techniques.
From discovery through trial, we provide the expert analysis and testimony you need to make your case.
Our proprietary methods uncover adverse event reports and complaints that traditional searches miss.
We connect the dots between relabeled devices and multiple manufacturers to reveal the full scope of harm.
Data integrity issues, falsified premarket data, safety signals—we find what others don't know exists.
Biocompatibility, toxicology, engineering, cybersecurity, usability, and more—we cover it all.
You're a law firm specializing in medical device product liability, medical malpractice defense, or False Claims Act matters. We're your ultimate case partners. You provide the legal representation. We'll take care of the rest.
Our expert network includes Subject Matter Experts in the following areas:
We find and build powerful cases against medical device companies:
Strengthen your defense with evidence that shifts liability:
Expose fraud with comprehensive regulatory analysis:
Making informed decisions about medical device safety and sourcing:
*It may be necessary to obtain premarket submission documents via FOIA request and/or discovery. See FAQ 12 for details.
Let's discuss what we can do for you.
Schedule a ConsultationDisclaimer: We cannot guarantee a particular outcome or verdict amount, what evidence we will find, or that we can identify every company associated with a particular device. Expert witness services are subject to availability. We are not a testing lab.