| Primary Device ID | B347BA5682101 |
| NIH Device Record Key | 5b73f705-17ae-4308-a2f4-aadb1bdc155d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Dr Dennis Gross Skincare |
| Version Model Number | BA568210 |
| Company DUNS | 197386191 |
| Company Name | LED TECHNOLOGIES INC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B347BA5682100 [Primary] |
| HIBCC | B347BA5682101 [Package] Contains: B347BA5682100 Package: [3 Units] In Commercial Distribution |
| HIBCC | B347BA5682102 [Package] Package: [8 Units] In Commercial Distribution |
| OHS | Light Based Over The Counter Wrinkle Reduction |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-02-20 |
| Device Publish Date | 2024-02-12 |
| B347BA5706101 | BA570610 |
| B347BA5688101 | BA568810 |
| B347BA5682101 | BA568210 |
| B347BA5681101 | BA568110 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() DR DENNIS GROSS SKINCARE 90498673 not registered Live/Pending |
DR. DENNIS GROSS SKINCARE, LLC 2021-01-29 |