device
FDA Expands Indication to BE for Magnetic Sphincter Augmentation Device
The FDA has expanded the indication for the magnetic sphincter augmentation device LINX to encompass patients with ...
AUGUST 19, 2024
FDA Clears AI Endoscopy Program
The FDA has granted 510(k) clearance to a new artificial intelligence program (CAD EYE, Fujifilm) to aid in ...
MARCH 21, 2024
Passive Monitoring Device Detects Crohn’s Activity
A monitoring device passively and accurately detects flares of Crohn’s disease before clinical signs appear, ...
SEPTEMBER 29, 2023
EndoHacks: Thinking Outside the Traditional Endoscopy Box
Optimizing Hemospray Delivery With Bone Wax
Hemostatic powder TC-325 (Hemospray, Cook Medical) is a highly effective primary and rescue noncontact hemostatic ...
JULY 14, 2022
Capsule Endoscopy: Past, Present, and Future
Since its introduction into clinical use in 2001, capsule endoscopy has been a game changer, enabling ...
MARCH 9, 2022
Novel Device Uses Mechanotransduction to Stimulate Tissue Growth and Treat Short Bowel Syndrome
Applying the concept of mechanotransduction to the small intestine in animal models, researchers have had success ...
FEBRUARY 28, 2022
Pentax Updates Duodenoscope Reprocessing Instructions
FDA recommends immediate training for ED-3490TK device
FEBRUARY 23, 2016
Senate Committee: Scope Outbreak Worse Than Reported
The global wave of “superbug” infections linked to contaminated duodenoscopes was much wider than ...
JANUARY 15, 2016