The U.S. Food and Drug Administration has approved Onapgo (apomorphine hydrochloride) injection as the first and only ...
The FDA has recalled Mercury Medical’s Neo-Tee T-Piece Resuscitator, a gas powered resuscitator intended primarily for ...
Our experts explain the science behind red light therapy, and if it really works. Plus, we recommend some FDA-cleared wands ...
Obesity-drug maker Metsera Inc.'s stock jumped 47% on Friday as the biggest gainer among three initial public offerings bucking a swoon in the equity market to rise in their stock-market debuts Friday ...
Similar signs of growth can be seen in the amount of drugs, biologics and medical devices the country exports to the US. The US FDA notes that China ranks third among countries that export drugs ...
Patient medical ... This drug has a similar chemical structure to sildenafil citrate and works in a similar manner. Tadalafil. Studies have indicated that tadalafil citrate stays in the body longer ...
FDA class 2 approved [510(k) number is K143690] exoskeleton (Ekso GTâ„¢, Ekso Bionics, Inc. Richmond, CA, USA). The RE is intended for overground gait rehabilitation under the guidance of a licensed ...
The Food and Drug Administration Feb. 5 released an alert notifying patients of a safety concern using diabetes devices such ...
A device long used by adults to manage migraines was now available for children as young as eight years old, offering new ...
Several executive orders recently signed by US President Donald Trump may have significant implications for the US Food and Drug Administration ...
The U.S. Food and Drug Administration has approved Supernus Pharmaceuticals' drug-device combination to treat ...
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