Implants

The CorNeat KPro implant is designed to replace deformed, scarred or opacified corneas and is expected to fully rehabilitate the vision of corneally blind patients immediately following implantation.

FDA approved Edwards Lifesciences' Konect Resilia aortic valved conduit, the first pre-assembled solution for Bentall procedures.

Canaccord Genuity's latest survey of orthopedic surgeons shows a "sharp bounce-back" in orthopedic surgery volumes, but the survey also raises concerns about sustainability, as COVID-19 rages on.

The Santa Clara, CA-based company said the study design would allow an initial analysis of safety and clinical efficacy for PMA submission after the first 250 patients have reached six months of follow-up, and then a second analysis after the...

The Lexington, MA-based company won an IDE from FDA to launch a pivotal trial of the study. Revita DMR is a same-day, outpatient endoscopic procedure that uses heat to resurface the lining of the upper intestine in a minimally invasive, outpatient...

A recent survey suggests that dentists should engage with patients on social media to share educational content, but that doesn't mean patients want to see images from bloody procedures in their newsfeeds.

FDA cited Allergan for failure to comply with post-approval study requirements. The agency also cited Ideal Implant for failures relating to quality system and medical device reporting regulations.