Law Firms | Reed Tech Navigator™ For Medical Devices

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

Simplify your litigation research

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.

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At a glance, Navigator can help:

Streamlined data management

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

Maintain a database with clean data

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

Find predicate devices easily

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

Access relevant data

Seamlessly identify applicable guidance documents

See what the competition is doing

Get competitive comparisons to understand safety and quality issues

Did you Know? Find Predicates and Successors with Reed Tech Navigator for Medical Devices. Watch the video now.

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.

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