FDA 510(k) Applications Submitted by STRAUMANN MANUFACTURING, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K080239 01/31/2008 P.004 ABUTMENTS, P.004 TEMPORARY COPINGS, P.004 PROTECTIVE CAPS, P.004 PERMANENT COPINGS STRAUMANN MANUFACTURING, INC.
K090260 02/03/2009 MODIFICATION TO:STRAUMANN GUIDED INSTRUMENTS STRAUMANN MANUFACTURING, INC.
K070478 02/20/2007 P.004 RC TEMPORARY ABUTMENT, P.004 TEMPORARY HEALING ABUTMENT (CAP) STRAUMANN MANUFACTURING, INC.
K092814 09/14/2009 STRAUMANN DENTAL ABUTMENTS STRAUMANN MANUFACTURING, INC.


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