| Primary Device ID | D707NA60504211 |
| NIH Device Record Key | cc408cbd-47aa-4b2f-930c-7b37121b215c |
| Commercial Distribution Discontinuation | 2023-08-28 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Valiant |
| Version Model Number | NA6050421 |
| Catalog Number | NA6050421 |
| Company DUNS | 176935203 |
| Company Name | IVOCLAR VIVADENT, INC. |
| Device Count | 500 |
| 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 | true |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | D707NA60504210 [Primary] |
| HIBCC | D707NA60504211 [Unit of Use] |
| EJJ | Alloy, amalgam |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-09-05 |
| Device Publish Date | 2023-08-28 |
| D707NA60501200 | NA6050120 |
| D707NA60501400 | NA6050140 |
| D707NA60501310 | NA6050131 |
| D707NA60502410 | Valiant Sure Cap No. 3 Econo |
| D707NA60504211 | Valiant Ph.D. No. 2 Econo |
| D707NA60501410 | NA6050141 |