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 |