Last synced on 18 April 2025 at 11:05 pm

Straumann BLX Ø3.5 mm Implants

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191256
510(k) Type
Traditional
Applicant
Institut Straumann AG
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
12/27/2019
Days to Decision
231 days
Submission Type
Summary

Straumann BLX Ø3.5 mm Implants

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191256
510(k) Type
Traditional
Applicant
Institut Straumann AG
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
12/27/2019
Days to Decision
231 days
Submission Type
Summary