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FDA Grants 510(k) Clearance for Innovative Fuse Gastroscope from EndoChoice
Date:10/28/2013

ology Week in Berlin, Germany. Researchers demonstrated the ability to see more with the Fuse system has a statistically significant impact on their ability to find adenomas or precancerous lesions when compared to traditional single-view endoscopes. "We have a national colorectal cancer screening program in the United States wherein most people should get screened for colorectal cancer, but not all patients follow these guidelines. The data from the Full Spectrum Endoscopy Tandem study would indicate that Fuse is a radical improvement over the tools we've used in the past to fight GI disease," said Douglas K. Rex, Professor of Medicine at Indiana University.

"We are 100% focused on serving the GI professionals so they can give the best possible care to their patients," said Mark Gilreath, Founder and CEO at EndoChoice. "This clearance by the FDA is yet another milestone in our efforts to make the Fuse system available to more hospitals and clinics."

About EndoChoice

Based in Atlanta, EndoChoice is a platform GI company that provides devices, diagnostics, infection control and imaging for specialists treating a wide range of gastrointestinal diseases. EndoChoice currently has over 2,000 customers and distribution in 34 countries worldwide, and has been recognized for four consecutive years as one of the fastest growing companies in the U.S. by Inc. Magazine. To learn more, visit www.endochoice.com.

EndoChoice and Fuse™ are trademarks of EndoChoice, Inc

For more information, press only:

Doug Ladd, Chief Marketing Officer
513-608-6873 or Doug.Ladd@endochoice.com

For more information on Fuse™


SOURCE EndoChoice
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