Our Expertise
and Regulatory Oversight

MAGUIRE Enterprises, Inc. is proud to share the FDA’s goal of assuring the safety and effectiveness of medical device products.

We were quick to act on the 1976 Medical Device Amendments to the FD&C Act and followed the guidelines needed for our manufacturing facility in Sunny South Florida to be registered as compliant. Since then our facility has effectively incorporated a quality assurance (QA) program, remaining steadfast in it’s mission to meet the Good Manufacturing Practice (GMP) requirements.

Today our rugged and reliable cables can be found throughout Critical Care, Cardiac, Emergency, Imaging and Surgical departments of hospitals across the nation. And most notably, there have been no reported events associated with our products.