Memic Receives FDA De Novo Marketing Authorization and launches a $96M round

Memic, a medical device company dedicated to transforming robot-assisted surgery with its proprietary technology, today announced that the U.S. Food and Drug Administration (FDA) has granted De Novo marketing authorization of its Hominis® robot-assisted surgical platform for use in single site, natural orifice laparoscopic-assisted transvaginal benign surgical procedures including benign hysterectomy. The De Novo authorization is supported by clinical data from procedures using the Hominis system on a variety of patients in Belgium and Israel.

Various press updates are available here, here, here and among other websites, here.


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