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FDA 510(k) Applications Submitted by GLIDEWELL LABORATORIES
FDA 510(k) Number
Submission Date
Device Name
Applicant
K060104
01/13/2006
PRISMATIK CLINICAL ZIRCONIA
GLIDEWELL LABORATORIES
K050144
01/24/2005
PRISMATIK CERAMIC
GLIDEWELL LABORATORIES
K972424
06/27/1997
SILENTNITE
GLIDEWELL LABORATORIES
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