# K032302: Xive TG Abutments

- Pathway: 510(k) (Traditional)
- Applicant: Friadent GmbH
- Decided: Oct 2, 2003 after 69 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
Longest line of descent: 5 generations back to K894595 (1990). 19 ancestors in all.
95 later devices descend from it; 5 cite it directly.
0 of 115 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K024004: Xive Transgingival Dental Implant System, Friadent GmbH (2003)
- K022859: Abutment and Prosthetic Accessories to the Iti Dental Implant System, Straumann USA (2002)

## Most influential descendants
- K040170: Friadent Plus Dental Implant Systems (2004), 84 descendants of its own
- K102804: Spi Titanium Base for Cad/Cam (2011), 83 descendants of its own
- K103691: Biohorizons Abutments for Zimmer (2011), 45 descendants of its own
- K112440: AB Dental Devices Implants and Accessories (2012), 36 descendants of its own
- K103291: Biohorizons Laser-Lok Abutments for Nobel Biocare (2011), 30 descendants of its own

## Indications for use
The XiVE@TG Abutment is intended for use to fabricate screw-retained or cementable crowns and bridges.

Source page: https://510kreport.com/device/K032302
Methodology: https://510kreport.com/methodology