Regulatory & Toxicology
Support

 

 

LEC Associates serves as a US agent for foreign medical device facilities and is a consultant for the development and filing of medical device registrations.

Services/Capabilities:

  • Registration of medical device facilities with the FDA
  • US FDA agent
  • Development of 510k, PMA and other device registration packages
  • Contract and monitoring of invitro, biocompatibility, acute and other toxicological testing to support device registrations