| Primary Device ID | 10841307118022 |
| NIH Device Record Key | acb2bbfd-42ae-4dc1-ad70-6d138f903aa7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UMA Titanium Temporary Hex Cylinder, .050"/1/25mm Hex Screw & Occlusal Plug |
| Version Model Number | 11-000302 |
| Catalog Number | 11-000302 |
| Company DUNS | 868856969 |
| Company Name | IMPLANT DIRECT SYBRON MANUFACTURING 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 | true |
| 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 |