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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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