# K971196: Endopore Endosseous Dental Implant System

- Pathway: 510(k) (Traditional)
- Applicant: Innova Corp.
- Decided: May 8, 1997 after 38 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.
9 later devices descend from it; 7 cite it directly.
0 of 10 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
- K032140: 5.0 X 5MM Endopore Endosseous Dental Implant System (2003), 6 descendants of its own
- K072425: Jne Implant System (2008), 1 descendant of its own
- 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

Source page: https://510kreport.com/device/K971196
Methodology: https://510kreport.com/methodology