Straumann USA, LLC (On Behalf of Institut Straumann Ag)
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories2
Latest FDA decision2020-08-19
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K200597 | Straumann BLX Gold Abutments | NHA | 2020-08-19 | View |
| 510(k) | K171757 | Straumann Screw Retained Abutments | NHA | 2017-11-27 | View |
| 510(k) | K171769 | Straumann PURE Ceramic Implants | DZE | 2017-11-14 | View |
No matching devices.