EGI is audited and certified annually to be in full compliance with ISO 13485:2003, an international standard which specifies requirements for a company-wide quality management system for manufacturers of medical devices and related services. EGI products meet all applicable medical device regulations in the United States, Canada, Japan, the European Community, and other locales.

For more information on EGI's products from the US Food and Drug Administration, use the links below.

For information on EGI's Financial Conflict of Interest Policy, use the links below.