The following data is part of a premarket notification filed by Kerr Corporation (danbury) with the FDA for Optibond.
Device ID | K940513 |
510k Number | K940513 |
Device Name: | OPTIBOND |
Classification | Agent, Tooth Bonding, Resin |
Applicant | KERR CORPORATION (DANBURY) 1332 SOUTH LONE HILL AVE. Glendora, CA 91740 |
Contact | Jeffrey A Anderson |
Correspondent | Jeffrey A Anderson KERR CORPORATION (DANBURY) 1332 SOUTH LONE HILL AVE. Glendora, CA 91740 |
Product Code | KLE |
CFR Regulation Number | 872.3200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-02-04 |
Decision Date | 1994-04-15 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
OPTIBOND 85007089 not registered Dead/Abandoned |
Bayer Aktiengesellschaft 2010-04-06 |
OPTIBOND 77053362 3346896 Dead/Cancelled |
LITEMAX ELECTRONICS INC. 2006-11-29 |
OPTIBOND 75619514 not registered Dead/Abandoned |
KEMIRA PAPER CHEMICALS CANADA INC. 1999-01-12 |
OPTIBOND 75388235 2482697 Live/Registered |
CORN PRODUCTS DEVELOPMENT, INC. 1997-11-12 |
OPTIBOND 75201029 2119642 Live/Registered |
Kerr Corporation 1996-11-20 |