| Primary Device ID | 00816131021889 |
| NIH Device Record Key | c648d76d-df04-4306-b1ed-f701e146f6cc |
| Commercial Distribution Discontinuation | 2016-12-29 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Rodo Abutment |
| Version Model Number | 53025NBA321 |
| Catalog Number | 53025NBA321 |
| Company DUNS | 004584361 |
| Company Name | RODO MEDICAL, 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 | true |
| 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 | true |
| OTC Over-The-Counter | false |