# K243824: Preat Abutments

- Pathway: 510(k) (Traditional)
- Applicant: Preat Corporation
- Decided: May 8, 2025 after 147 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: 18 generations back to K960026 (1996). 357 ancestors in all.
No later device cites it as a predicate yet.
0 of 358 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K220823: Preat Abutments, Preat Corporation (2022) Summary page 6.

## Indications for use
Preat Abutments are intended to be used in conjunction with endosseous dental implants in the maxillary or mandibular arch to provide support for single-unit or multi-unit prosthetic restorations. All digitally designed CAD/CAM customizations for Preat Abutments are intended to be sent to a Preat validated Milling Center for manufacture or to be designed and manufactured according to a validated digital dentistry workflow. The workflow system integrates multiple components of the digital dentistry workflow: scan files from intra-oral and lab (desktop) scanners, CAD software, CAM software, milling machine and associated tooling and accessories. Preat Abutments are compatible with the following third-party implant restorative platforms:

Source page: https://510kreport.com/device/K243824
Methodology: https://510kreport.com/methodology