This site uses modern web standards that aren't supported by your browser. For best results, please upgrade to Google Chrome, Microsoft Edge, or Mozilla Firefox.

Law Firms

Law Firms

Law Firms

Find the best predicates for your client’s 510(k) applications and discover & monitor safety events

When supporting your medical device clients, in-depth, accurate research is invaluable in all facets of litigation and applications. However, databases are often unorganized, not standardized and difficult to filter and compare. With this in mind, Reed Tech has developed a solution that allows you to find the best, relevant predicates to push FDA applications through quickly and seamlessly – and compares the safety and quality data of any device to its competitors and the industry averages in an effort to simplify litigation research.

Gain medical device insights today with Navigator for
Medical Devices

Instant access to search by FDA Product Code, Manufacturer Name, Intended Use, and more

2 Day Trial. Ready To Get Started?

At a glance, Navigator can help:

Quickly see safety trends with connected
and normalized data—all in one place


Trust that you have access to clean data to
understand reported product problems,
adverse event reports, recalls and their causes


Identify the best predicate device – search 510(k)s by intended use, indication for use, and more


Seamlessly identify applicable
guidance documents


Get competitive comparisons to
understand safety and quality issues

Did you know? Find Predicates and Successors


Free Trial of Navigator

Access to search by FDA Product Code, Manufacturer Name, Intended Use, and more:

  • Product Search: search by K Number, PMA Number and Device Type with advanced filtering to refine results.
  • Clearance Search: quickly search by K Number, De Novos Number, Device Description, or Intended Use/Indication for Use, a feature only found in Navigator.
  • Adverse Events: search by Report Number, MDR Report Key or Initial Event Date with additional filters to refine results sets.
  • Watchlists: monitor new events for selected products or separately, for selected clearances.

Understand the trends for medical safety and quality—then use that knowledge to better inform risk management, product design, market research, post-market surveillance and regulatory intelligence.





By continuing to use the site, you agree to the use of cookies. more information

The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.