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ENT
FDA Clears Expanded Indication of Acclarent AERA® Eustachian Tube Balloon Dilation System
Procedures may now be performed on patients as young as 18. New data on local anesthesia also recognized
Long-Term Data Confirm Durable Relief of Nasal Obstruction Symptoms with Latera®
Patients who benefitted from Latera experienced continued symptom relief after the implant had absorbed
MEDICA 2017 Sees Launch of Single-Use Diathermy Abbey Needle with Suction
New device reduces risk of cross contamination and unintentional patient burns from damaged insulation
Positive Clinical Study Results for Nasal Valve Collapse Implant
Newly presented prospective multi-center study yields significant reduction in nasal obstruction symptoms
First US Cases for MIS Nasal Valve Collapse Device
Newly cleared minimally invasive device for lateral cartilage support in patients with nasal valve collapse, a major cause of nasal obstruction
Medtronic’s NuVent™ Indications Expanded to Include Revision Sinus Surgery
Clinical study conducted on revision subjects supports expanded indication for patients with previously surgically altered tissue
FDA Clears Cochlear’s First Smart Bone Conduction Solution
System works for people with significant mixed hearing loss
Study of New Steroid-Eluting Spacer Assesses FESS Outcomes
Comparative study will assess improvement in patient outcomes from avoidance of steroid bolus
FDA Clearance for Medrobotics® Flex® Robotic System
“I’ve been a surgeon since 1960 and this technology is one of the most significant operating room advances I’ve seen in decades”
CE Mark for SinuSys™ Vent-Os® Sinus Dilation System for Treatment of Frontal and Sphenoid Sinusitis
Two new devices will expand portfolio of low-pressure, self-expanding dilation devices to treat frontal and sphenoid sinusitis, in addition to maxillary disease.
Lumenis Touts its Dual CO2 Laser for Challenging Cases: Symposium at COSM
Lumenis sees its dual CO2 laser technology featured at this week’s Combined Otolaryngology Spring Meetings (COSM) in Boston
New Study Investigates Sinus Surgery Outcomes Using Steroid-Eluting Spacer
SinuSys Corporation is to commence a new clinical trial of its proprietary drug-eluting spacer, infused with steroids for use following functional endoscopic sinus surgery (FESS)
First MRI-Conditional Cochlear Implant Approved in U.S.
MED-EL USA has announced U.S. FDA approval of its new SYNCHRONY cochlear implant, the first time such a device has been approved for use with 3.0 Tesla MRI without the surgical removal of the internal magnet.
Medtronic Launches Chitosan-Based Nasal Packing and Stent for FESS
FDA cleared back in October, Medtronic is now to launch its Novashield, Chitosan-Based material for use in Functional Endoscopic Sinus Surgery.
Pentax Medical Launches New VIVIDEO ENT System in EMEA Markets
New Pentax ENT Videoscope Delivers a “Different World” of Image and Illumination