FDA 510(k) Applications Submitted by WHIP MIX CORPORATION

FDA 510(k) Number Submission Date Device Name Applicant
K190107 01/22/2019 VeriSplint Whip Mix Corporation
K152443 08/27/2015 Vericore Gradient Temporary Disc WHIP MIX CORPORATION
K142670 09/19/2014 Vericore Zirconia Blanks WHIP MIX CORPORATION


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