# K251471: IPD Dental Implant Abutments

- Pathway: 510(k) (Traditional)
- Applicant: Implant Protesis Dental 2004, S.L.
- Decided: Aug 20, 2025 after 99 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: 23 generations back to K960026 (1996). 324 ancestors in all.
No later device cites it as a predicate yet.
0 of 325 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K242819: IPD Dental Implant Abutments, Implant Protesis Dental 2004, S.L. (2024) Summary page 6.

## Indications for use
IPD Dental Implant Abutments are intended to be used in conjunction with endosseous dental implants in the maxillary or mandibular arch to provide support for single or multiple dental prosthetic restorations. The zirconia superstructures for use with the Ti Base (Interface) are only intended to be designed and manufactured according to digital dentistry workflow. The workflow system integrates multiple components of the digital dentistry workflow: scan files from intra-oral scanners, CAD software, CAM software, ceramic material, milling machine and associated tooling and accessories.

Source page: https://510kreport.com/device/K251471
Methodology: https://510kreport.com/methodology