| Primary Device ID | D9493180210 |
| NIH Device Record Key | f365f982-af53-48ab-b17b-a2ee6cda4c7c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Biofit HD Matrix |
| Version Model Number | 5.5 mm Molar |
| Company DUNS | 059020838 |
| Company Name | Bioclear Matrix Systems |
| Device Count | 50 |
| 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 | true |
| 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 |