The following data is part of a premarket notification filed by Premier Dental Products Co. with the FDA for Zytron.
Device ID | K780796 |
510k Number | K780796 |
Device Name: | ZYTRON |
Classification | Material, Tooth Shade, Resin |
Applicant | PREMIER DENTAL PRODUCTS CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | EBF |
CFR Regulation Number | 872.3690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1978-05-15 |
Decision Date | 1978-06-22 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ZYTRON 87442632 5830877 Live/Registered |
Zytron, Inc. 2017-05-09 |
ZYTRON 77082799 not registered Dead/Abandoned |
BFS Brands, LLC 2007-01-15 |
ZYTRON 76392555 2948774 Live/Registered |
KAPPLER, INC. 2002-04-09 |
ZYTRON 76292538 2604474 Live/Registered |
Zytron Control Products, Inc. 2001-08-01 |
ZYTRON 73685370 1485937 Dead/Cancelled |
ZYTRON SPORTS INJURY PRODUCTS, INC. 1987-09-21 |