Author: iData Research
Zimmer Biomet Trauma Implants Cleared the CE Mark, but will an FDA Approval Follow?
Zimmer Biomet’s Bactiguard-coated orthopedic trauma implants have recently received European regulatory clearance and CE mark. Preparations for registering the implants in the U.S. market are also o... Read More
DePuy Synthes Receives 510(k) FDA Clearance for VELYS™ Robotic-Assisted Solution
DePuy Synthes has recently announced they received 510(k) FDA Clearance for VELYS, a robotic-assisted system designed for use with the Attune total knee system. DePuy Synthes has described the Velys p... Read More
Breakthrough FDA Approval for ACL Tears to be Healed Instead of Being Rebuilt
The U.S. Food and Drug Administration recently granted marketing authorization for an anterior cruciate ligament (ACL) implant, intended to perform as an alternative to traditional ACL reconstructions... Read More
Remote Patient Monitoring is Rapidly Growing in Mainstream Healthcare
The U.S. market for patient monitoring devices and equipment includes products that are designed to measure and observe changes in vital signs or the neurological, homodynamic, and cardiac functions o... Read More
BioSerenity Announces FDA Clearance for Electroencephalography (EEG) Wearable Device System
BioSerenity, Inc., recently announced they received U.S. Food and Drug Administration (FDA) 510(k) clearance for the Neuronaute® Electroencephalography (EEG) System and IceCap® EEG wearable device t... Read More
Can AI Help Improve In-Vitro Fertilization Rates?
Although in vitro fertilization solely involves a sperm and an egg, the process leading to an embryo can be more challenging than just putting the two together. In 2019, the Centers for Disease Contro... Read More
Over 190,000 Atherectomy Procedures Performed Every Year In The United States
According to a new atherectomy market study by iData Research, over 190,000 atherectomy procedures are performed each year in the United States. Atherectomy is a procedure that consists of removing at... Read More
Medtronic’s MIS Drill Received FDA Approval Ahead Of Schedule
Medtronic has announced that the U.S. Food and Drug Administration (FDA) has cleared the use of navigated interbody high-speed drills with the Robotic Guidance System. Even in the midst of the COVID19... Read More
