FDA 510(k) Applications Submitted by U & I CORPORATION

FDA 510(k) Number Submission Date Device Name Applicant
K180759 03/22/2018 SECULOKÖ Suture Anchor U & I Corporation
K131200 04/29/2013 ASPIRON ACP SYSTEM U & I CORPORATION
K132797 09/06/2013 L'DISQ U & I CORPORATION
K183383 12/06/2018 ANAXÖ OCT Spinal System U & I Corporation
K132101 07/08/2013 ANAX 5.5 SPINAL SYSTEM U & I CORPORATION
K132218 07/17/2013 PERFIX ILIAC SCREW SYSTEM U & I CORPORATION
K143631 12/22/2014 Benefix Interspinous Fixation System U & I Corporation


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