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 |