Search results
FX Shoulder obtains FDA 510(k) clearance for glenoid baseplates
Medical Device Network via Yahoo Finance· 36 minutes agoFX Shoulder Solutions has secured 510(k) clearance from the US Food and Drug Administration (FDA)...
Amgen’s IMDELLTRA receives FDA approval for lung cancer treatment
Pharmaceutical Technology via Yahoo Finance· 1 hour agoAmgen has announced the US Food and Drug Administration's (FDA) accelerated approval for its...
Claritas HealthTech’s iPETcertum device to extend Claritas iPET capability
Medical Device Network via Yahoo Finance· 16 minutes agoClaritas said that the Claritas iPET, which already obtained US Food and Drug Administration (FDA)...
Louisiana may reclassify drugs used in abortion as controlled dangerous substances
NPR· 37 minutes agoMifepristone and misoprostol have many clinical uses, but one FDA-approved use is to take the pills...
FDA approves self-collection screening tests for HPV, allowing women to avoid pelvic exams for...
FierceBiotech· 2 days agoThe FDA has approved two diagnostic devices that allow women to collect vaginal samples themselves...
FDA greenlights self-collection of vaginal samples for cervical cancer screening
KMBC-TV Kansas City· 15 hours agoTwo health care businesses – biotechnology company Roche and medical technology firm Becton, Dickson...
FDA APPROVES IMDELLTRA™ (TARLATAMAB-DLLE), THE FIRST AND ONLY T-CELL ENGAGER THERAPY FOR THE...
FOX 5 San Diego· 11 hours agoAmgen (NASDAQ:AMGN) today announced that the U.S. Food and Drug Administration (FDA) has approved IMDELLTRA™ (tarlatamab-dlle) for the treatment of adult patients with extensive-stage ...
FDA Approves Tarlatamab for Extensive-Stage SCLC
Medscape· 1 day agoContinued approval of the first-in-class bispecific T-cell engager (BiTE) may depend on proof of clinical benefit.
Small Business - The Brewton Standard | The Brewton Standard
The Brewton Standard· 1 hour agoBrainomix Achieves Breakthrough with FDA Clearance of e-Lung AI Software PR Newswire OXFORD, England, and CHICAGO, May 17, 2024 Established market leader in stroke AI imaging ...
FDA said it never inspected dental lab that made controversial AGGA device
Medical Xpress· 22 hours agoThe FDA never inspected Johns Dental Laboratories during more than a decade in which it made the...