FDA 510(k) Applications Submitted by Genicon, Inc

FDA 510(k) Number Submission Date Device Name Applicant
K180579 03/05/2018 Ezee Retrieval Genicon, Inc
K180836 03/30/2018 Genistrong Genicon, Inc
K171752 06/13/2017 X-SURGE Genicon, Inc
K181791 07/05/2018 SIMPLYSTRONG, SIMPLYEZEE Genicon, Inc
K162059 07/26/2016 EZEE RETRIEVAL GENICON, INC


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