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FDA 510(k) Applications Submitted by David Elier
FDA 510(k) Number
Submission Date
Device Name
Applicant
K150296
02/06/2015
Biodenta Customized Abutment-Hybrid
BIODENTA SWISS AG
K151295
05/15/2015
Biodenta Customized Abutment - Titanium
BIODENTA SWISS AG
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