| Primary Device ID | D090800025720 |
| NIH Device Record Key | 815685cd-0723-4c6b-8fb2-89c91ebe1b68 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DEXIS Ti2 Sensor |
| Version Model Number | 8.000.2572 |
| Company DUNS | 800111106 |
| Company Name | Dental Imaging Technologies Corporation |
| 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 | false |
| Lot Batch | false |
| Serial Number | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | D090800025720 [Primary] |
| MUH | System, X-Ray, Extraoral Source, Digital |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-12-20 |
| Device Publish Date | 2023-12-12 |
| D090100879340 - DEXIS 10 (DEXIS Imaging Suite) | 2024-03-20 |
| D090800025750 - DEXIS Ti2 Sensor Kit | 2024-01-31 DEXIS Ti2 Kit, EN FR-CA |
| D090800025780 - DEXIS Ti2 Sensor Kit | 2024-01-31 DEXIS Ti2 Warranty Replacement NEW |
| D090800025790 - DEXIS Ti2 Sensor Kit | 2024-01-31 Upgrade Kit, Sensor to Ti2 |
| D090800025800 - DEXIS Ti2 Sensor Kit | 2024-01-31 DEXIS Ti2 Warranty Replacement - R |
| D090800025840 - DEXIS Ti2 Sensor Kit | 2024-01-31 Upgrade Kit, Platinum to Ti2 |
| 00693856000302 - CS MODEL+ | 2023-12-21 LICENCE CS MODEL+ V5 ALIGNER CAPABILITY |
| D090800025720 - DEXIS Ti2 Sensor | 2023-12-20 |
| D090800025720 - DEXIS Ti2 Sensor | 2023-12-20 |