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FDA 510(k) Applications Submitted by Ana C.M. 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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