| Primary Device ID | 00810044841367 |
| NIH Device Record Key | 423f9108-0b33-411f-b81a-f172dd747111 |
| Commercial Distribution Discontinuation | 2020-03-05 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | OsseoFuse HexaPlus Sinus Dental Implant |
| Version Model Number | SLF4510 |
| 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 |