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FDA 510(k) Applications Submitted by EST. ANTHOGYR
FDA 510(k) Number
Submission Date
Device Name
Applicant
K020431
02/08/2002
FIBIOCORE
EST. ANTHOGYR
K070084
01/09/2007
MONTBLANC IMPLANTOLOGY CONTRA ANGLE CONTROL
EST. ANTHOGYR
K060317
02/08/2006
ANTHOGYR CONTRA ANGLES AND HANDPIECES
EST. ANTHOGYR
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