FDA 510(k) Applications Submitted by BIORENEW LABS, LLC

FDA 510(k) Number Submission Date Device Name Applicant
K152889 09/30/2015 SONILASE BLUE, SONILASE BLUE-CLEAN, SONILASE BLUE-UV CLEAN PLUS BIORENEW LABS, LLC
K132613 08/21/2013 SONILASE LIGHT THERAPY DEVICE BIORENEW LABS, LLC


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