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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