| Primary Device ID | D7911900B3500 |
| NIH Device Record Key | 42b964a1-cbbe-4c66-8d2c-0e3ec369f1c8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Luminesse Low Fusing Porcelain |
| Version Model Number | 1900B350 |
| Company DUNS | 094430642 |
| Company Name | TALLADIUM, 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 | D7911900B3500 [Primary] |
| EIH | Powder, Porcelain |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-07-24 |
| Device Publish Date | 2016-10-24 |
| D7911900T1500 | 1900T150 |
| D7911900ST4500 | 1900ST450 |
| D7911900ST3500 | 1900ST350 |
| D7911900ST2500 | 1900ST250 |
| D7911900ST1500 | 1900ST150 |
| D7911900D4500 | 1900D450 |
| D7911900D3500 | 1900D350 |
| D7911900C4500 | 1900C450 |
| D7911900C3500 | 1900C350 |
| D7911900C2500 | 1900C250 |
| D7911900C1500 | 1900C150 |
| D7911900B4500 | 1900B450 |
| D7911900B3500 | 1900B350 |
| D7911900B2500 | 1900B250 |
| D7911900B1500 | 1900B150 |
| D7911900B0500 | 1900B050 |
| D7911900B00500 | 1900B0050 |
| D7911900A4500 | 1900A450 |
| D7911900A35500 | 1900A3550 |
| D7911900A3500 | 1900A350 |
| D7911900A2500 | 1900A250 |
| D7911900A1500 | 1900A150 |
| D7911900A0500 | 1900A050 |
| D7911900A00500 | 1900A0050 |