| Primary Device ID | D724D4407260 | 
| NIH Device Record Key | 45d704fb-aba2-4151-97a9-bc11bd960dbc | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Vivid TempFill LC | 
| Version Model Number | D440746 | 
| 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 | D724D4407260 [Primary] | 
| EBF | Material, Tooth Shade, Resin | 
| 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 | 2016-06-28 | 
| 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 |