The following data is part of a premarket notification filed by Vident with the FDA for Vita In-ceram.
| Device ID | K913644 |
| 510k Number | K913644 |
| Device Name: | VITA IN-CERAM |
| Classification | Powder, Porcelain |
| Applicant | VIDENT 5130 COMMERCE DR. Baldwin Park, CA 91706 |
| Contact | Ray E Morrow |
| Correspondent | Ray E Morrow VIDENT 5130 COMMERCE DR. Baldwin Park, CA 91706 |
| Product Code | EIH |
| CFR Regulation Number | 872.6660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-08-16 |
| Decision Date | 1992-06-22 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() VITA IN-CERAM 73789835 1599446 Live/Registered |
VITA ZAHNFABRIK H. RAUTER GMBH & CO. KG 1989-03-29 |