More than 1,300 Chinese medical-device companies that registered to sell protective gear and other equipment in the U.S. during the coronavirus pandemic listed as their American representative a ...
Entries include information on each product, their manufacturer and date of the agency's approval. New tobacco products that received marketing authorization through one of FDA's three pathways to ...
Due to policies regarding industry user fees, the FDA will not be able to accept any new drug applications for the duration ...
WASHINGTON, November 26 - As the Food and Drug Administration (FDA) suspended the food facility registration of Portales, New Mexico-based Sunland Inc. Monday, worldwide concerns began to spread about ...
In the ever-changing regulatory landscape that alcohol manufacturers must navigate, the regulations imposed by the U.S. Food and Drug Administration (FDA) are often overlooked. But breweries, ...
LAUSANNE, Switzerland--(BUSINESS WIRE)--Abionic SA, a developer of disrupter nanotechnology based rapid diagnostic solutions, announced today that its rapid allergy test, IVD CAPSULE Aeroallergens, ...
Augmedics has received the Food and Drug Administration (FDA) 510(k) clearance of the new CT-to-fluoroscopy (CT-Fluoro) registration method for its xvision spine system. Navigating off using ...
PARIS--(BUSINESS WIRE)--Inotrem, an advanced clinical stage biotech company specializing in immunotherapies for acute and chronic inflammatory syndromes, today announced the outcome of its regulatory ...
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