| Primary Device ID | 00810044840971 |
| NIH Device Record Key | 8e391503-b892-4e57-a317-169b2eec8c50 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Osseofuse HexaPLUS Dental Implant |
| Version Model Number | HFCA-HS |
| Company DUNS | 080694564 |
| Company Name | OSSEOFUSE INTERNATIONAL, 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 | 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 |