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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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