| Primary Device ID | 00810027861566 |
| NIH Device Record Key | 17bb5aef-8bad-42b2-8256-a77541a7d15b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Bone Level Implant |
| Version Model Number | I3132160 |
| Company DUNS | 026108395 |
| Company Name | I3 IMPLANT LLC |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |