The FDA extended the duration of use of Nexplanon for pregnancy prevention in women of reproductive potential for up to 5 years.

Spine Innovation’s Logic titanium implant system earned FDA 510(k) clearance, according to a Jan. 26 news release. The device is the next generation of the company’s implant system which has been used ...

“The Enlighten study is a real world experience of what happens to patients who get this device,” said Dr. Theodore Takata, a ...

The U.S. Food and Drug Administration (FDA) has granted 510 (k) clearance for updated labeling of a resorbable implant for anterior cruciate ligament (ACL) repair, indicating a reduced risk of ...

Cortigent is a leading developer of brain interface devices based on precision neurostimulation technology The company’s new ...

BCI® Therapy is being developed to restore thought-driven movement in people living with spinal cord injuries and other ...

Organon’s Nexplanon can now be implanted for up to five years after the FDA approved a supplemental New Drug Application by ...

Cresco Spine announced that the U.S. FDA has granted 510(k) clearance for the Spring Distraction System (SDSTM), for the ...

The DETECT study is the first randomised controlled trial comparing Minder System implants to standard care monitoring.

Participants in a deep brain stimulation trial for drug addiction say the implants triggered compulsive behavior that upended ...

Lung imaging house 4D Medical this week is finalising its monster $150 million fund raising for a "once in a generation" US ...