510K Clearance for X-Surge Product Group

X-Surge Instrument

GENICON announced today that the U.S. Food and Drug Administration has granted 510(k) clearance for the Company’s X-Surge product group.  This clearance extends GENICON’s portfolio of advanced laparoscopic Electro-Surgical Instrumentation (ESI) which now includes economically friendly single use shafts and actuating tips to work in concert with reusable handle assemblies along with the Company’s award winning complete single use instrumentation.


Designed with surgeon-directed enhancements, the X-Surge product group will now provide the global healthcare community with a comprehensive array of choices in their approach to meeting surgeons needs with laparoscopic ESI products.


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