Endoscopy

CMS Postponing Non-Essential Medical, Surgical, and Dental Procedures

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CMS Postponing Non-Essential Medical, Surgical, and Dental Procedures

CMS Postponing Non-Essential Medical, Surgical, and Dental ProceduresAt the White House Task Force Press Briefing last week, the Center for Medicare & Medicaid Services (CMS) announced that all non-essential medical, surgical and dental procedures would be postponed until further notice in order to shift priorities to treating those affected by the coronavirus outbreak. The decision

iData ResearchCMS Postponing Non-Essential Medical, Surgical, and Dental Procedures
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PENTAX Launches IMAGINA LED Powered Endoscopy System

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PENTAX Launches IMAGINA LED Powered Endoscopy System

Pentax launches IMAGINA LED Powered Endoscopy System for ambulatory surgery centers in the U.S. after winning FDA clearance. The LEDs mounted on the tip do not require regular replacement eliminating the need for expensive replacement bulbs. The ultra-bright in conjunction with the real-time integrated i-SCAN Image Enhancement system allows for a high-resolution image of mucosal

iData ResearchPENTAX Launches IMAGINA LED Powered Endoscopy System
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Check-Cap Announces Positive Results from Pilot Study of New Capsule Endoscopy System

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Check-Cap Announces Positive Results from Pilot Study of New Capsule Endoscopy System

After conducting a pilot study in the U.S., Check-Cap announces their positive results attained for their C-Scan System. The C-Scan system is the first and only preparation-free ingestible scanning capsule-based system that aids in the prevention of colorectal cancer through the detection of precancerous polyps. The open label, single arm study was designed to evaluate

iData ResearchCheck-Cap Announces Positive Results from Pilot Study of New Capsule Endoscopy System
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PENTAX Duodenoscope FDA Cleared

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PENTAX Duodenoscope FDA Cleared

Featuring a sterile, disposable distal cap PLUS disposable elevator, is the DEC HD Duodenoscope. This new device from Pentax Medical was recently cleared by the FDA in the United States. With its disposable components, the HD DEC Duodenoscope will help reduce the risk of bioburden remaining on conventional elevator components after reprocessing. On top of

iData ResearchPENTAX Duodenoscope FDA Cleared
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C.R. Bard Hernia Repair Device FDA Cleared

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C.R. Bard Hernia Repair Device FDA Cleared

Register to receive a free Soft Tissue Repair Market Analysis, Size and Trends Report synopsis and brochure. The Phasix ST Mesh also comes with the Echo 2 Positioning System for ventral hernia repair as a secondary option to a permanent mesh. This system allows for a more accurate and reliable mesh placement for minimally invasive

iData ResearchC.R. Bard Hernia Repair Device FDA Cleared
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Soft Tissue Hernia Mesh from Exogenesis FDA Cleared

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Soft Tissue Hernia Mesh from Exogenesis FDA Cleared

Register to receive a free Soft Tissue Repair Market Analysis, Size, and Trends Report synopsis and brochure. Exogenesis, a developer of proprietary nanoscale surface modification and surface announced a new milestone in hernia repair. Their Exogenesis nanoMesh recently received clearance from the FDA. The soft tissue repair implant is designed to facilitate tissue ingrowth to

iData ResearchSoft Tissue Hernia Mesh from Exogenesis FDA Cleared
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Intersect ENT’s Investigational Drug-Coated Balloon Results

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Intersect ENT’s Investigational Drug-Coated Balloon Results

Register to receive a free U.S. ENT Devices Market Analysis, Size and Trends Report synopsis and brochure. Results of a new balloon dilation device study in the ENT market have been released. The ASCEND drug-coated sinus balloon from Intersect ENT is currently in investigational use only by federal law. The devices safety and efficacy were

iData ResearchIntersect ENT’s Investigational Drug-Coated Balloon Results
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FUJIFILM’S Endoscopic Imaging Solutions FDA Cleared

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FUJIFILM’S Endoscopic Imaging Solutions FDA Cleared

Register to receive a free U.S. Gastrointestinal Endoscopic Devices Market Analysis, Size, and Trends Report synopsis and brochure. In a recent approval from the FDA, Fujifilm Medical Systems 6 new endoscopic imaging solutions have received clearance. These new GI and interventional endoscopy devices have increased the portfolio of Fujifilm’s offerings. The 6 new endoscopes imaging

iData ResearchFUJIFILM’S Endoscopic Imaging Solutions FDA Cleared
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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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