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FDA 510(k) Applications Submitted by SUNSTAR AMERICAS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K102053
07/22/2010
BUTLER CALCI-FLOR PROPHYLAXIS PASTE
SUNSTAR AMERICAS, INC.
K132325
07/26/2013
GUIDOR BIORESORBABLE MATRIX BARRIER
SUNSTAR AMERICAS, INC.
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