| Primary Device ID | G5103268 |
| NIH Device Record Key | dd2e11c4-08c9-47b8-a369-8c8d685367df |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SUNTAN SUPPLY |
| Version Model Number | 3268 |
| 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 | G5103268 [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 | 2025-08-21 |
| Device Publish Date | 2025-08-13 |
| G5103268 | 3268 |
| G5103248 | 3248 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SUNTAN SUPPLY 90109324 not registered Live/Pending |
JLW-TW CORP 2020-08-12 |
![]() SUNTAN SUPPLY 76239050 2835765 Dead/Cancelled |
JLW-TW CORP 2001-04-10 |