The following data is part of a premarket notification filed by Vericom Co., Ltd. with the FDA for Spacer.
Device ID | K072069 |
510k Number | K072069 |
Device Name: | SPACER |
Classification | Material, Tooth Shade, Resin |
Applicant | VERICOM CO., LTD. 27001 LA PAZ ROAD, SUITE 312 Mission Viejo, CA 92691 |
Contact | Albert Rego |
Correspondent | Albert Rego VERICOM CO., LTD. 27001 LA PAZ ROAD, SUITE 312 Mission Viejo, CA 92691 |
Product Code | EBF |
CFR Regulation Number | 872.3690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-07-30 |
Decision Date | 2007-09-28 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SPACER 98486883 not registered Live/Pending |
Sanctives Group, Inc. 2024-04-05 |
SPACER 98152855 not registered Live/Pending |
Chikviladze, Zurabi 2023-08-28 |
SPACER 80993900 0993900 Dead/Cancelled |
Electronic Associates, Inc. 0000-00-00 |
SPACER 75119728 2079047 Live/Registered |
Lutron Electronics Co., Inc. 1996-06-17 |
SPACER 74698218 not registered Dead/Abandoned |
Dimensional Technology International, Inc. 1995-06-30 |
SPACER 74242817 1721996 Dead/Cancelled |
EAC Corporation 1992-02-03 |
SPACER 73753899 1606347 Dead/Cancelled |
SUPERWOUND LIMITED 1988-09-26 |
SPACER 73571381 1434659 Dead/Cancelled |
SUPERWOUND LIMITED 1985-12-02 |
SPACER 73308507 not registered Dead/Abandoned |
SOUND TECHNOLOGY, INC. 1981-05-04 |