Tag: Food and Drug Administration (FDA)
First Patients in the World Treated with Impella RP Flex with SmartAssist
DANVERS, Mass.--(BUSINESS WIRE)-- Abiomed (Nasdaq: ABMD) announces the first three patients in the world have been treated with Impella RP Flex with SmartAssist, Abiomed’s...
WISE obtains FDA approval for new neuromonitoring device
<!----> Medical device firm WISE has received US Food and Drug Administration (FDA) approval for its WISE Cortical...
Elon Musk says Neuralink’s brain chip to begin human trials in 6 months
Elon Musk is known to work at least 16 hours a day. While working tirelessly to revamp Twitter after acquiring the social giant for...
IN-FOCUS: Lazurite
<!----> Rankings 2022 INNOVATION – CommendedPRODUCT LAUNCHES – CommendedRESEARCH AND DEVELOPMENT – Commended Medical Device Network Excellence Awards and Rankings 2022 –...
HemoSonics receives FDA 510(k) market clearance for Quantra System
<!----> US-based medical device firm HemoSonics has received 510(k) market clearance for its Quantra Hemostasis System with QStat...
The Real Reason Marijuana Isn’t Fully Legalized in America, Yet.
The REAL REASON why weed isn’t fully legalized yet… One would think that with 7 out of 10 Americans in favor of cannabis legalization...
ANANDA Scientific Announces FDA Approval of the IND for a Clinical Trial exploring treatment of Social Anxiety Disorder (SAD)
NEW YORK & GREENWOOD VILLAGE, Colo.–(BUSINESS WIRE)–ANANDA Scientific Inc., a research focused bio-pharmaceutical company today announced approval by the US Food and Drug Administration...
Smartphone-based diagnosis to promote the early detection of chronic diseases
<!-- --> Mobile health (mHealth) refers to mobile devices, including smartphones and tablets, that are used alongside software...
NanoVibronix Receives FDA 510(k) Premarket Clearance for PainShield Plus
ELMSFORD, N.Y.--(BUSINESS WIRE)-- NanoVibronix, Inc., (NASDAQ: NAOV), a medical device company utilizing the Company's proprietary and patented low intensity surface acoustic wave (SAW) technology,...
AnchorDx enrols first participant for UriFind assay trial in US
Chinese cancer early detection solutions developer AnchorDx has enrolled the first participant in the clinical trial of its...
FDA Sends Warning Letters To Companies Selling CBD-Infused Foods And Beverages As Hemp Industry Awaits Regulations
The Food and Drug Administration (FDA) has sent warning letters to five companies that sell foods and beverages containing CBD—the agency’s latest stepped-up enforcement...
Zimmer Biomet obtains FDA 510(k) clearance for Persona OsseoTi Keel Tibia
Medical technology firm Zimmer Biomet has received 510(k) clearance for its Persona OsseoTi Keel Tibia from the US...
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