FDA 510(k) Applications Submitted by VIVORTE, INC

FDA 510(k) Number Submission Date Device Name Applicant
K143547 12/15/2014 Vivorte Trabexus EB VIVORTE, INC
K143549 12/15/2014 Vivorte Trabexus VIVORTE, INC
K130703 03/15/2013 VIVORTE BVF VIVORTE, INC
K131133 04/23/2013 VIVORTE BVF LITE VIVORTE, INC


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