| Primary Device ID | D7911900C2500 | 
| NIH Device Record Key | b2a50f50-2538-44a2-a382-9de6e6336e5a | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Luminesse Low Fusing Porcelain | 
| Version Model Number | 1900C250 | 
| 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 | D7911900C2500 [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 |