| Primary Device ID | G51023450 |
| NIH Device Record Key | 5df34a03-d354-4c37-bbe1-a94edc837c84 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BE BRIGHT |
| Version Model Number | 2345 |
| Company DUNS | 075058495 |
| Company Name | Light Sources, 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 | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | G51023450 [Primary] |
| LEJ | Booth, Sun Tan |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-09-06 |
| Device Publish Date | 2024-08-29 |
| G51023610 | 2361 |
| G51023520 | 2352 |
| G51023630 | 2363 |
| G51023510 | 2351 |
| G51023450 | 2345 |
| G5102346 | 2346 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BE BRIGHT 97286813 not registered Live/Pending |
The Key Clinic Limited 2022-02-28 |
![]() BE BRIGHT 87007770 5219702 Live/Registered |
Retail Royalty Company 2016-04-20 |
![]() BE BRIGHT 86549197 4952709 Live/Registered |
The Coromega Company, Inc. 2015-02-27 |
![]() BE BRIGHT 86090168 4607185 Live/Registered |
Gonzalez, Yuisa 2013-10-12 |
![]() BE BRIGHT 85483501 4287724 Live/Registered |
Gap (Apparel), LLC 2011-11-30 |
![]() BE BRIGHT 79167888 4943691 Live/Registered |
GrandVision Group Holding B.V. 2015-03-03 |
![]() BE BRIGHT 78100689 2762866 Dead/Cancelled |
CONAIR CIP, INC. 2002-01-03 |