# K926354: Endo-Pore Endosseous Dental Implant System

- Pathway: 510(k) (Traditional)
- Applicant: Innova Corp.
- Decided: Feb 13, 1995 after 784 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.
5 later devices descend from it; 4 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K043190: Scalloped Endopore Endosseous Dental Implant System (2004), 1 descendant of its own
- K040714: Hybrid Endopore Endosseous Dental Implant (2004), 1 descendant of its own
- K113113: Endosseous Dental Implant (2012), 0 descendants of its own
- K052951: Endopore Anatomic Endosseous Dental Implant System (2006), 0 descendants of its own
- K042971: Titan Dental Implant System (2005), 0 descendants of its own

Source page: https://510kreport.com/device/K926354
Methodology: https://510kreport.com/methodology