Friday, September 23, 2022
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Medical Devices

FDA Grants QT Imaging Clearance to Calculate Fibroglandular Volume of the Breast

The U.S. Food and Drug Administration (FDA) has granted QT Imaging, Inc. 510(K) clearance to calculate the fibroglandular volume (FGV) of the breast and...

Brooks Rehabilitation Participates in National Stroke Recovery Trial Using Breakthrough Technology

Brooks Rehabilitation first participant in the national stroke recovery trial, EMAGINE, has just completed study participation. The randomized, double-blind study tests whether a non-invasive,...

Centinel Spine Announces First Commercial Use of the prodisc C Vivo Cervical Total Disc Replacement System in the Western U.S.

Centinel Spine, LLC, a leading global medical device company addressing cervical and lumbar spinal disease through anterior surgical access, announced the first implantation of...

Guerbet announces U.S. Food and Drug Administration (FDA) approval of Elucirem

Guerbet (FR0000032526 GBT), a global leader in medical imaging, announced that the U.S. Food and Drug Administration (FDA) after priority review, approved Elucirem (Gadopiclenol),...

Stryker receives FDA clearance for OptaBlate Bone Tumor Ablation System

Stryker, one of the world's leading medical technology companies, announced that its OptaBlate bone tumor ablation system (OptaBlate) received 510(k) clearance from the U.S....

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