| Primary Device ID | D724S2702701 |
| NIH Device Record Key | 8b76d268-7ec1-471e-82da-b1596d76ce53 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vivid Root MTA |
| Version Model Number | S270270 |
| Company DUNS | 082874108 |
| Company Name | PEARSON DENTAL SUPPLIES, 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 | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | D724S2702701 [Primary] |
| KIF | Resin, Root Canal Filling |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-09-22 |
| Device Publish Date | 2016-06-30 |
| D724D0104501 - Vivid Surebond VII | 2024-02-16 |
| D724D0104521 - Vivid Surebond VII Refill | 2024-02-16 |
| D724S2702601 - Vivid Ceramic Prime | 2024-02-16 |
| D724B0105080 - Vivid Electrode Tip #11 | 2023-04-04 |
| D724B8805000 - Vivid Surgo Matic | 2023-04-04 |
| D724B8805020 - Vivid Electrode Tip #1 | 2023-04-04 |
| D724B8805040 - Vivid Electrode Tip #2 | 2023-04-04 |
| D724B8805060 - Vivid Electrode Tip #6 | 2023-04-04 |