| Primary Device ID | 00408939 |
| NIH Device Record Key | 0fb2d4e3-70c1-4b75-a7c8-2d97acd94283 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VTRAC |
| Version Model Number | 100-120 Vac Credit |
| Company DUNS | 618522536 |
| Company Name | Strata Skin Sciences, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | 00408939 [Primary] |
| GEX | Powered Laser Surgical Instrument |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-12-21 |
| Device Publish Date | 2017-02-13 |
| 00408939 | 100-120 Vac Credit |
| 00408919 | 100-120 Vac Non Credit |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() VTRAC 85614806 4404191 Live/Registered |
Optovue, Inc. 2012-05-02 |
![]() VTRAC 78269943 not registered Dead/Abandoned |
VTrac Systems, Inc. 2003-07-02 |
![]() VTRAC 78269937 2961055 Dead/Cancelled |
VTrac Systems, Inc. 2003-07-02 |
![]() VTRAC 77505837 3567548 Live/Registered |
STRATA SKIN SCIENCES, INC. 2008-06-23 |
![]() VTRAC 77201009 3404601 Dead/Cancelled |
Applied Vision Corporation 2007-06-08 |