FDA clears next-gen handheld ultrasound from Butterfly Network
January 8, 2024
Butterfly Network (NYSE:BFLY) announced today that it received FDA clearance for its next-generation handheld ultrasound system.
Butterfly Network (NYSE:BFLY) announced today that it received FDA clearance for its next-generation handheld ultrasound system.
Medtronic (NYSE: MDT)+
today announced FDA approval of its Percept RC deep brain stimulation system, the latest member of its Percept line of DBS devices.
Zoll this week announced it received FDA clearance and CE mark approval for upgrades to its Thermogard temperature management system
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.
Siemens Healthineers announced today that the FDA cleared its Magnetom Cima.X 3 Tesla (3T) magnetic resonance imaging whole-body scanner.
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™
Johnson & Johnson MedTech unit Acclarent announced that it won a new FDA clearance for its Aera Eustachian tube balloon dilation system.
ALWAY, Ireland–(BUSINESS WIRE)– Perfuze, a private medical device company dedicated to developing pioneering technology to treat acute ischemic stroke, proudly announces FDA clearance for the Millipede 070 Aspiration Catheter and the 2nd generation of the Millipede 088 Access Catheter.