Renovos secures FDA breakthrough status for bone graft alternative
January 5, 2024
When injected, Renovite acts as a scaffold for cells and helps localize and retain molecules that stimulate healing
When injected, Renovite acts as a scaffold for cells and helps localize and retain molecules that stimulate healing
The company’s continuous blood pressure monitor allows clinical investigators to remotely capture data on patients.
Medtronic (NYSE: MDT)+
announced today that it received CE mark approval for its next-generation Micra AV2 and Micra VR2 miniature, leadless pacemakers.
Imagine electrostatic materials that function even with extremely weak ultrasound, heralding the era of permanent implantable electronic devices in biomedicine.
A research team from Odense University Hospital and the University of Southern Denmark has developed an innovative screening test. With a blood sample from the expectant mother, they can scrutinize all the genes in the fetus.
Siemens Healthineers announced today that the FDA cleared its Magnetom Cima.X 3 Tesla (3T) magnetic resonance imaging whole-body scanner.
iRhythm Technologies (Nasdaq: IRTC)+
announced today that it received CE mark for its Zio system and its supporting Zeus AI algorithm.
EndoSound announced today that it received FDA 510(k) clearance for its EndoSound Vision System (EVS).
FDA clearance supported by highly compelling clinical study results demonstrating 93% of subjects treated arms were “improved” or “very much improved” in appearance, following treatment utilizing SUPERB™
Swallowing the device before a meal could create a sense of fullness, tricking the brain into thinking it’s time to stop eating.