# K093708: Telio Cad

- Pathway: 510(k) (Traditional)
- Applicant: Ivoclar Vivadent, Inc.
- Decided: Mar 10, 2010 after 98 days
- Product code: EBG (Crown And Bridge, Temporary, Resin)
- Device class: 2
- Regulation: 21 CFR 872.3770
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
11 later devices descend from it; 5 cite it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K113739: Simplant Immediate Smile Dental Care System (2012), 3 descendants of its own
- K172281: PuRE PMMA Disc (2017), 2 descendants of its own
- K170849: SIMPLANT Guide (2017), 2 descendants of its own
- K151564: Telio CAD Abutment Solutions (2015), 1 descendant of its own
- K261456: Ruthinium Disc (2026), 0 descendants of its own

## Indications for use
For the fabrication of temporary crowns and bridges using the CAD/CAM technology until the permanent restoration can be delivered.

Source page: https://510kreport.com/device/K093708
Methodology: https://510kreport.com/methodology