FDA 510(k) Applications Submitted by Ana Vianna

FDA 510(k) Number Submission Date Device Name Applicant
K223083 09/30/2022 Straumann SLActive labeling changes Institut Straumann AG
K191256 05/10/2019 Straumann BLX ╪3.5 mm Implants Institut Straumann AG
K190040 01/08/2019 Straumann BLX Line Extension - New Abutments Institut Straumann AG
K193046 11/01/2019 Straumann« Retentive System û Novaloc TiN Abutments Institut Straumann AG


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