The following data is part of a premarket notification filed by Dental Direkt Gmbh with the FDA for Dd Cubex2 Hs.
| Device ID | K170885 |
| 510k Number | K170885 |
| Device Name: | DD CubeX2 HS |
| Classification | Powder, Porcelain |
| Applicant | Dental Direkt GmbH Industriezentrum 106-108 Spenge, DE 32139 |
| Contact | Uwe Greitens |
| Correspondent | Uwe Greitens Dental Direkt GmbH Industriezentrum 106-108 Spenge, DE 32139 |
| Product Code | EIH |
| CFR Regulation Number | 872.6660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-03-27 |
| Decision Date | 2017-08-01 |