Primary Device ID | 00887661525215 |
NIH Device Record Key | 15dc6ee7-c215-4e95-b612-a6cbeaf69590 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FALLS CREEK |
Version Model Number | 10241240.FMR |
Company DUNS | 062312087 |
Company Name | FGX INTERNATIONAL INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | +1(401)231-3800 |
Customerservices@fgxi.com | |
Phone | +1(401)231-3800 |
Customerservices@fgxi.com | |
Phone | +1(401)231-3800 |
Customerservices@fgxi.com | |
Phone | +1(401)231-3800 |
Customerservices@fgxi.com | |
Phone | +1(401)231-3800 |
Customerservices@fgxi.com | |
Phone | +1(401)231-3800 |
Customerservices@fgxi.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887661525215 [Primary] |
HQY | Sunglasses (non-prescription including photosensitive) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-06-30 |
Device Publish Date | 2022-06-22 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FALLS CREEK 77844051 3881285 Live/Registered |
Meijer, Inc. 2009-10-08 |
FALLS CREEK 75807218 not registered Dead/Abandoned |
Del Webb Corporation 1999-09-23 |
FALLS CREEK 75640570 2324035 Live/Registered |
MEIJER, INC. 1999-02-12 |
FALLS CREEK 75009662 2001553 Live/Registered |
Meijer, Inc. 1995-10-10 |
FALLS CREEK 73464243 1319510 Live/Registered |
Meijer, Inc. 1984-02-06 |