BRANEMARK SYSTEM
Implant, Endosseous, Root-form
NOBELPHARMA USA, INC.
The following data is part of a premarket notification filed by Nobelpharma Usa, Inc. with the FDA for Branemark System.
Pre-market Notification Details
| Device ID | K934825 |
| 510k Number | K934825 |
| Device Name: | BRANEMARK SYSTEM |
| Classification | Implant, Endosseous, Root-form |
| Applicant | NOBELPHARMA USA, INC. 5101 S. KEELER AVE. Chicago, IL 60632 |
| Contact | Alan I Becker |
| Correspondent | Alan I Becker NOBELPHARMA USA, INC. 5101 S. KEELER AVE. Chicago, IL 60632 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-10-08 |
| Decision Date | 1994-08-08 |
Trademark Results [BRANEMARK SYSTEM]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 BRANEMARK SYSTEM 74486952 1917780 Dead/Cancelled |
NOBELPHARMA AB 1994-02-04 |
 BRANEMARK SYSTEM 73671730 1587384 Live/Registered |
NOBELPHARMA AB 1987-07-13 |
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