FDA 510(k) Applications Submitted by Straumann USA, LLC (on behalf of Institut Straumann AG)
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K171757 | 06/14/2017 | Straumann Screw Retained Abutments | Straumann USA, LLC (on behalf of Institut Straumann AG) |
| K171769 | 06/14/2017 | Straumann PURE Ceramic Implants | Straumann USA, LLC (on behalf of Institut Straumann AG) |
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