Private certification, insurer evaluation and peer-reviewed research step up.
Stereotaxis Inc. (NYSE: STXS), St. Louis-based developer of robotic technologies to treat arrhythmias and perform ...
Leading securities law firm Bleichmar Fonti & Auld LLP announces that a class action lawsuit has been filed against Inspire Medical Systems, Inc. (NYSE: INSP) and certain of the Company's senior ...
A few weeks ago, the FDA issued what is known as a safety communication related to Radiofrequency (RF) Microneedling devices ...
Myomo ranks at the top for Revenue Growth and Gross Profit among its peers. However, it ranks at the bottom for Return on ...
The IDE approval marks a pivotal milestone for Aqua Medical, allowing the company to begin enrolling patients in the U.S. RESTORE-1 pilot trial and study PIMA's potential to deliver durable metabolic ...
Aqua Medical has received investigational device exemption (IDE) from the FDA for its ablation device aimed at treating ...
The U.S. Food and Drug Administration (FDA) is warning consumers, patients and health care providers about the potential risk ...
SAN FRANCISCO, Oct. 30, 2025 /PRNewswire/ -- Sirona Medical today announced that it has received U.S. Food and Drug Administration (FDA) 510(k) clearance for its Sirona Advanced Imaging Suite, marking ...
BrainCheck, a digital cognitive assessment and care platform that includes an FDA Class II medical device (BrainCheck Assess(TM)), today announced the completion of a three-year project expanding its ...
The cervical disc replacement landscape just got a major upgrade. The FDA has officially granted premarket approval (PMA) for two-level indications for not one, but two total disc replacement (TDR) ...
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