The following data is part of a premarket notification filed by Ivoclar Vivadent Ag with the FDA for Ips Ivocolor.
| Device ID | K151894 |
| 510k Number | K151894 |
| Device Name: | IPS Ivocolor |
| Classification | Powder, Porcelain |
| Applicant | IVOCLAR VIVADENT AG BENDERERSTRASSE 2 Schaan, LI Fl-9494 |
| Contact | Sandra Cakebread |
| Correspondent | Donna Hartnett IVOCLAR VIVADENT, INC. 175 PINEVIEW DRIVE Amherst, NY 14228 |
| Product Code | EIH |
| CFR Regulation Number | 872.6660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-07-10 |
| Decision Date | 2015-10-29 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() IPS IVOCOLOR 87446556 not registered Live/Pending |
Ivoclar Vivadent, Inc. 2017-05-11 |