FDA Clears Marketing of PatchAssist Laparoscopic Hernia Mesh Placement Device
Israel’s PolyTouch Medical has received FDA clearance to market its PatchAssist laparoscopic hernia mesh placement device. The tool was developed to allow surgeons a more predictable and standardized approach to apply hernia patches. PatchAssist easily unfolds the mesh inside the abdominal cavity, accurately places the mesh over the hernia defect and enables surgeon to verify the mesh position before attachment is made. Patch Assist does not change laparoscopic techniques used today by surgeons, rather it eliminates manual, complicated, and time consuming tasks.
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PolyTouch Medical Ltd. Receives FDA Clearance to Commercialize PatchAssist(TM)
Atrium Medical receives FDA nod for two new Omega 3 surgical mesh products
SafeStitch Medical, Inc. Receives FDA Clearance to Market the AMID StaplerTM for Hernia Repairs
Bovie laparoscopic SEER device approved
Covidien receives FDA nod for surgery kit for laparoscopic procedures
