# K130829: IQ Implants; IQ Implants; IQ Implants Abutments

- Pathway: 510(k) (Traditional)
- Applicant: Iq Implants, Ltd.
- Decided: Nov 14, 2013 after 233 days
- Product code: DZE (Implant, Endosseous, Root-Form)
- Device class: 2
- Regulation: 21 CFR 872.3640
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K151169: OsteoReady ZircoSeal Abutments (2015), 0 descendants of its own

## Indications for use
IQ Implant System Is Indicated for use In surgical and restorative applications for placement In the bone of the upper or lower jaw to provide support for prosthetic devices, such as artificial teeth. In order to restore the patients chewing function. IQ Implant System is Indicated also for Immediate loading when good primary stability Is achieved and with appropriate occlusai loading.

Source page: https://510kreport.com/device/K130829
Methodology: https://510kreport.com/methodology