Country for PR: United States
Contributor: PR Newswire New York
Tuesday, April 19 2022 - 22:00
AsiaNet
SMART Medical Systems' G-EYE (R) Colonoscope is now FDA Cleared on Olympus' PCF Colonoscope Series, Making it Available in the United States on the Commonly Used Models of All Leading Endoscopy Brands
RA'ANANA, Israel, April 19, 2022 /PRNewswire-AsiaNet/ --

- FDA has approved the use of G-Eye (R) with Olympus' 510(k) cleared PCF 
colonoscopes –

SMART Medical Systems Ltd., a developer and manufacturer of innovative 
endoscopy products, today announced an additional FDA clearance for its G-EYE 
(R) Colonoscope, based on Olympus' 510(k) cleared PCF colonoscope series. With 
this additional FDA clearance, G-EYE (R) is now available for use in the U.S. 
market on the commonly used colonoscope models of all three leading endoscopy 
brands - OLYMPUS, FUJIFILM, and PENTAX Medical.

Logo - https://mma.prnewswire.com/media/1669152/smart_Logo.jpg

"The ability to offer G-EYE (R) on colonoscope brands and models commonly used 
and widely available in the United States is an important milestone for SMART 
Medical, patients, and endoscopists," said Gadi Terliuc, Chief Executive 
Officer of SMART Medical. "The majority of U.S. endoscopists now have the 
option to utilize our cutting-edge technology, which has been shown in clinical 
studies to improve visualization compared with standard colonoscopy, while 
using their preferred brand and model of colonoscope. We are very excited to 
have completed our portfolio of U.S. G-EYE (R) offerings and believe that the 
widespread availability of the technology on the commonly used colonoscope 
models has the potential to accelerate adoption of G-EYE (R) colonoscopy as the 
standard of care."

The G-EYE (R) Colonoscope is a 510(k) cleared colonoscope, remanufactured by 
SMART to include a proprietary balloon at its distal bending section. 
Withdrawal of the G-EYE (R) Colonoscope with the balloon moderately inflated 
during colonoscopy assists in controlling the colonoscope's field of view and 
positioning. A published study (GIE 2019; 89: 545-53) demonstrated that G-EYE 
(R) can improve colonoscopy outcomes compared with standard colonoscopy across 
several metrics, including increasing adenoma detection rate (ADR) by 28%, 
detecting 47% more adenomas per patient (APP), 62% more advanced and large 
adenomas, and 142% more flat adenomas.

"We expect that this FDA clearance of the G-EYE (R) Colonoscope based on 
Olympus' PCF scopes, which many Olympus users prefer over traditional 
adult-sized colonoscopes, will enhance our ability to capture a substantial 
portion of the U.S. colonoscopy market," said Brian Cochrane, Chief Commercial 
Officer of SMART's U.S. subsidiary. "We are committed to becoming the standard 
of care in colonoscopy, and this FDA clearance is an important step toward 
achieving this critical goal."

About SMART Medical Systems
SMART Medical Systems is a pioneer in the development and manufacture of 
innovative medical devices in the field of gastro-intestinal (GI) endoscopy. 
SMART's unique approach is to address key challenges in contemporary endoscopy 
while using available brand name endoscopes. SMART's CE Marked and FDA-cleared 
NaviAid (TM) and G-EYE (R) product families are commercially distributed in key 
global markets. With its partnership with FUJIFILM and PENTAX Medical, SMART's 
G-EYE (R) colonoscopy solution is currently adopted by two of the three 
industry leaders in GI endoscopy imaging. SMART is headquartered in Israel, and 
operates in the United States through its wholly-owned subsidiary, SMART GI 
Inc. For more information, please visit: www.smartmedsys.com/us/.

Media Contact:
Glenn Silver, Lazar FINN
Glenn.silver@finnpartners.com
+1 (973) 818-8198

SOURCE: SMART Medical Systems
Translations

Japanese