| Primary Device ID | 10190730084566 |
| NIH Device Record Key | bb94e341-ab34-4660-8f9c-ddf204d74d2e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Clear Advantage |
| Version Model Number | 7500-035 |
| Company DUNS | 781772017 |
| Company Name | ORTHO TECHNOLOGY, INC. |
| Device Count | 25 |
| DM Exempt | true |
| Pre-market Exempt | true |
| 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 | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00190730084569 [Primary] |
| GS1 | 10190730084566 [Unit of Use] |
| KMY | POSITIONER, TOOTH, PREFORMED |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-08-01 |
| Device Publish Date | 2025-07-24 |
| 10190730084573 | Splint Material .080“ 25 sheets per pack |
| 10190730084566 | Splint Material .060“ – FOIL packaging of 25 |
| 10190730084559 | Splint Material .040“ 50 sheets per pack |
| 10190730084542 | Splint Material .030“ – FOIL packaging of 50 |
| 10190730084535 | Splint Material .020“ 50 sheets per pack |