| Primary Device ID | EDET045871 |
| NIH Device Record Key | d2baf8e0-53c0-447b-80f1-d12b883faea2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VITA VIONIC® TRY-IN RESIN A2 1000g |
| Version Model Number | 04587 |
| Company DUNS | 343947949 |
| Company Name | DETAX GmbH |
| 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 | false |
| Expiration Date | true |
| 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 | EDET045871 [Primary] |
| KMY | Positioner, Tooth, Preformed |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-06-23 |
| Device Publish Date | 2025-06-13 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() VITA VIONIC 86092388 4647782 Live/Registered |
Vita Zahnfabrik H. Rauter GmbH & Co. KG 2013-10-15 |