# K043190: Scalloped Endopore Endosseous Dental Implant System

- Pathway: 510(k) (Special)
- Applicant: Innova Life Sciences Corp.
- Decided: Dec 14, 2004 after 27 days
- Product code: NHA (Abutment, Implant, Dental, Endosseous)
- Device class: 2
- Regulation: 21 CFR 872.3630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K971196 (1997). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K926354: Endo-Pore Endosseous Dental Implant System, Innova Corp. (1995) Summary page 1.
- K971196: Endopore Endosseous Dental Implant System, Innova Corp. (1997) Summary page 1.
- K032140: 5.0 X 5MM Endopore Endosseous Dental Implant System, Innova Life Sciences Corp. (2003) Summary page 1.

## Most influential descendants
- K052951: Endopore Anatomic Endosseous Dental Implant System (2006), 0 descendants of its own

## Indications for use
For use as an endosseous dental implant in the upper or lower jaw arches to provide support for prosthetic devices.

Source page: https://510kreport.com/device/K043190
Methodology: https://510kreport.com/methodology