The following data is part of a premarket notification filed by Degussa Ag with the FDA for Degubond Ultra.
| Device ID | K953344 |
| 510k Number | K953344 |
| Device Name: | DEGUBOND ULTRA |
| Classification | Alloy, Gold-based Noble Metal |
| Applicant | DEGUSSA AG 3900 SOUTH CLINTON AVE. South Plainfield, NJ 07080 |
| Contact | Holger Meinicke |
| Correspondent | Holger Meinicke DEGUSSA AG 3900 SOUTH CLINTON AVE. South Plainfield, NJ 07080 |
| Product Code | EJT |
| CFR Regulation Number | 872.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-07-12 |
| Decision Date | 1995-08-25 |