Gastrointestinal

Olympus Launches “PowerSpiral”, World’s First Motorized Rotation Endoscope in Europe and Asia

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Olympus Launches “PowerSpiral”, World’s First Motorized Rotation Endoscope in Europe and Asia

Register to receive a free U.S. Market Report Suite for Gastrointestinal Endoscopic Devices – MedSuite report synopsis and brochure On March 29th 2019, Olympus Corporation announced that “PowerSpiral” endoscopy system will be introduced to Europe and parts of Asia-Pacific. In the future, “PowerSpiral” will launch in the United States and other parts of the Asia-Pacific region when certifications

iData ResearchOlympus Launches “PowerSpiral”, World’s First Motorized Rotation Endoscope in Europe and Asia
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U.S. Gastrointestinal Endoscopic Device Market Projected to Reach $3.7 Billion by 2025- New Study by iData Research

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U.S. Gastrointestinal Endoscopic Device Market Projected to Reach $3.7 Billion by 2025- New Study by iData Research

VANCOUVER, British Columbia–(BUSINESS WIRE)–According to the latest suite of reports by iData Research, the United States gastrointestinal (GI) endoscopic device market was valued at over $2.9 billion in 2018, and is expected to exceed $3.7 billion by 2025. The total market value includes, GI endoscopes, capsule endoscopy, virtual colonoscopy software, stenting and dilation devices, endoscopic

iData ResearchU.S. Gastrointestinal Endoscopic Device Market Projected to Reach $3.7 Billion by 2025- New Study by iData Research
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MIT Develops Expanding Monitoring Capsule Pill

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MIT Develops Expanding Monitoring Capsule Pill

Register to receive a free U.S. Market Report Suite for Gastrointestinal Endoscopic Devices – MedSuite report synopsis and brochure Engineers at MIT have developed an inflatable ingestible capsule for continuous long-term stomach monitoring. The pill’s materials are designed such that it can be easily swallowed by the patient and inflate quickly in the stomach to a size

iData ResearchMIT Develops Expanding Monitoring Capsule Pill
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Actuated Medical, Inc. Receives Innovative Technology Contract from Vizient, Inc. for the TubeClear System

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Actuated Medical, Inc. Receives Innovative Technology Contract from Vizient, Inc. for the TubeClear System

Register to receive a free U.S. Market Report Suite for Gastrointestinal Endoscopic Devices – MedSuite report synopsis and brochure Actuated Medical, Inc. announced its TubeClear System has received an Innovative Technology contract from Vizient, Inc., the largest member-driven health care performance improvement company in the country. The contract was based on a recommendation of the TubeClear System

iData ResearchActuated Medical, Inc. Receives Innovative Technology Contract from Vizient, Inc. for the TubeClear System
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Motus GI Receives FDA Clearance to Market Pure-Vu® Slim Sleeve for Use with Slim Colonoscopes

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Motus GI Receives FDA Clearance to Market Pure-Vu® Slim Sleeve for Use with Slim Colonoscopes

Register to receive a free U.S. Market Report Suite for Gastrointestinal Endoscopic Devices – MedSuite report synopsis and brochure Motus GI Holdings, Inc., (“Motus GI” or the “Company”), a medical technology company dedicated to improving clinical outcomes and enhancing the cost-efficiency of colonoscopy, announced that it has received special 510(k) clearance from the U.S. Food and Drug

iData ResearchMotus GI Receives FDA Clearance to Market Pure-Vu® Slim Sleeve for Use with Slim Colonoscopes
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An Astounding 16.6 Million Colonoscopies are Performed Annually in The United States

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An Astounding 16.6 Million Colonoscopies are Performed Annually in The United States

An analysis of endoscopic gastrointestinal procedure volumes by iData Research shows that over 16.6 million colonoscopies will be performed annually by 2019, significantly contributing to the 28 million gastrointestinal endoscopies performed each year in the United States. A major factor driving growth in colonoscopy procedures is the increasing public awareness of colon cancer, through media

iData ResearchAn Astounding 16.6 Million Colonoscopies are Performed Annually in The United States
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Apollo Endosurgery Receives Special 510(k) Clearance for OverStitch™ Sx Endoscopic Suturing System

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Apollo Endosurgery Receives Special 510(k) Clearance for OverStitch™ Sx Endoscopic Suturing System

Register to receive a free U.S. Market Report Suite for Gastrointestinal Endoscopic Devices – MedSuite report synopsis and brochure Apollo Endosurgery, Inc., a global leader in less invasive medical devices for bariatric and gastrointestinal procedures, announced that it has received Special 510(k) clearance from the U.S. Food and Drug Administration for OverStitch™ Sx Endoscopic Suturing System. The

iData ResearchApollo Endosurgery Receives Special 510(k) Clearance for OverStitch™ Sx Endoscopic Suturing System
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Swallowable Device Detects Pre-Cancerous Barrett’s Esophagus

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Swallowable Device Detects Pre-Cancerous Barrett’s Esophagus

Register to receive a free U.S. Market Report Suite for Gastrointestinal Endoscopic Devices 2017 – MedSuite report synopsis and brochure Researchers have developed a test for early detection of an esophageal adenocarcinoma precursor lesion that uses a swallowable balloon to collect DNA samples from the bottom of the esophagus, according to a report published in Science Translation

iData ResearchSwallowable Device Detects Pre-Cancerous Barrett’s Esophagus
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TRICOR-Systems Inc. Launches Dri-Scope Aid®2 with Dual Timer to Assist in the Drying of the Internal Channels of an Endoscope

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TRICOR-Systems Inc. Launches Dri-Scope Aid®2 with Dual Timer to Assist in the Drying of the Internal Channels of an Endoscope

TRICOR-Systems Inc. is excited to announce the new Dri-Scope Aid®2 with dual timer. The dual timer will allow the operator to hook up two endoscopes (Olympus, Pentax, and Fuji) with independent start and stop times.

iData ResearchTRICOR-Systems Inc. Launches Dri-Scope Aid®2 with Dual Timer to Assist in the Drying of the Internal Channels of an Endoscope
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