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Zacks Small Cap Research on MSNMGRM: Monogram Receives Clearance from the FDA on its 510(k) Submission for its mBôs TKA System.MGRM READ THE FULL MGRM RESEARCH REPORT On March 17, 2025, Monogram (NASDAQ:MGRM) announced that the FDA has granted 510(k) clearance for its Monogram mBôs TKA System. This determination means that ...
Creative Medical Technology Holdings announced that the U.S. Food and Drug Administration has cleared an expanded dose escalation for its ongoing Phase 1/2 trial of StemSpine usin ...
Ionis Pharma's olezarsen has become the first FDA-approved drug therapy for adults ... The drug – formerly known as IONIS-APOCIII-LRx – has been cleared under the Tryngolza brand name as ...
Monogram Technologies secured 510(k) clearance for its robotic knee replacement system, while Vicarious Surgical blamed ...
This FDA clearance for the Magstim Horizon 3.0 and Inspire systems builds on the existing patient TMS clearances for adult patients, making it possible for physicians and nurse practitioners to treat ...
The PGA Tour has cleared Wyndham Clark of a rules violation after the former US Open champion took a free drop during the second round of the Arnold Palmer Invitational at Bay Hill. Clark ...
The agency updates and modifies the alerts as needed. Recent modifications to FDA’s import alerts, as posted by the agency, are listed below. Click here to go to the FDA page with links to ...
The US Food and Drug Administration (FDA) has granted clearance to Qiagen’s QIAstat-Dx Gastrointestinal Panel 2 Mini B, expanding the company’s syndromic testing offerings in the US.
The FDA cleared the investigational new drug application for MRANK-106, a dual WEE1/YES1 kinase inhibitor, targeting advanced solid tumors. The FDA has cleared the investigational new drug (IND) ...
The latest authorised panel targets bacterial infections, including Campylobacter, Shigella, Yersinia enterocolitica, and Salmonella. Credit: © Qiagen. The US Food ...
The Persona Knee system. [Image courtesy of Zimmer Biomet] Zimmer Biomet (NYSE: ZBH) + announced today that it received FDA 510(k) clearance for its Persona Revision SoluTion Femur. The revision ...
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