Kyphoplasty systems
DIOnavi. Abutment Jig
A device intended to be used as a copy of a dental implant, for a dental laboratory working model, to duplicate the location and restorative platform orientation of the final dental implant; it is not intended for intraoral use. It is a rod-like device made of metal [e.g., titanium (Ti)]. This is a single-use device.
Where to buy DIOnavi. Abutment Jig
We do not have contact details for DIO Corporation yet. Send a request and we will route it to the right person for your country.
DIOnavi. Abutment Jig models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| AJ3D 05 | — | Not stated | Available |
Procedures that use kyphoplasty systems
Frequently asked questions
What is DIOnavi. Abutment Jig used for?
A device intended to be used as a copy of a dental implant, for a dental laboratory working model, to duplicate the location and restorative platform orientation of the final dental implant; it is not intended for intraoral use. It is a rod-like device made of metal [e.g., titanium (Ti)]. This is a single-use device.
Who makes DIOnavi. Abutment Jig?
DIOnavi. Abutment Jig is made by DIO Corporation. It is listed under vertebral augmentation systems (kyphoplasty and vertebroplasty) in our device library.
What sizes does DIOnavi. Abutment Jig come in?
The FDA device database does not list sizes for DIOnavi. Abutment Jig. Check the instructions for use or ask a DIO Corporation representative.
Is DIOnavi. Abutment Jig MRI safe?
The FDA device database entry for DIOnavi. Abutment Jig does not state its MRI safety status. Check the labeling before MRI.
Is DIOnavi. Abutment Jig FDA cleared?
DIOnavi. Abutment Jig is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a DIO Corporation sales representative?
DIO Corporation has not listed representatives on LA Vascular yet. Visit the DIO Corporation company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.