BONDING BASE
Implant, Endosseous, Root-form
STRAUMANN USA
The following data is part of a premarket notification filed by Straumann Usa with the FDA for Bonding Base.
Pre-market Notification Details
| Device ID | K973353 |
| 510k Number | K973353 |
| Device Name: | BONDING BASE |
| 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 | 1997-09-05 |
| Decision Date | 1997-12-02 |
| Summary: | summary |
Trademark Results [BONDING BASE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BONDING BASE 74603401 not registered Dead/Abandoned |
MERCER GROUP LTD, THE 1994-11-28 |
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