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FDA 510(k) Applications Submitted by Straumann USA, LLC (on behalf of Institut Straumann AG)
FDA 510(k) Number
Submission Date
Device Name
Applicant
K171757
06/14/2017
Straumann Screw Retained Abutments
Straumann USA, LLC (on behalf of Institut Straumann AG)
K171769
06/14/2017
Straumann PURE Ceramic Implants
Straumann USA, LLC (on behalf of Institut Straumann AG)
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