ITI DENTAL IMPLANT SYSTEM
Implant, Endosseous, Root-form
STRAUMANN USA
The following data is part of a premarket notification filed by Straumann Usa with the FDA for Iti Dental Implant System.
Pre-market Notification Details
| Device ID | K030007 |
| 510k Number | K030007 |
| Device Name: | ITI DENTAL IMPLANT SYSTEM |
| Classification | Implant, Endosseous, Root-form |
| Applicant | STRAUMANN USA RESERVOIR PLACE, 1601 TRAPELO ROAD Waltham, MA 02154 |
| Contact | Linda Jalbert |
| Correspondent | Linda Jalbert STRAUMANN USA RESERVOIR PLACE, 1601 TRAPELO ROAD Waltham, MA 02154 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-01-01 |
| Decision Date | 2003-03-31 |
| Summary: | summary |
Trademark Results [ITI DENTAL IMPLANT SYSTEM]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ITI DENTAL IMPLANT SYSTEM 75614838 2454453 Dead/Cancelled |
Institut Straumann AG 1999-01-04 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.