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 |