# K141457: Dentium Implantium and Superline Abutments

- Pathway: 510(k) (Abbreviated)
- Applicant: Dentium Co., Ltd.
- Decided: Nov 12, 2014 after 163 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: 8 generations back to K944964 (1995). 45 ancestors in all.
6 later devices descend from it; 4 cite it directly.
0 of 52 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K041368: Dentium CO., LTD. Implantium, Dentium Co., Ltd. (2004) Summary page 4.
- K052823: Implantium Abutments, Dentium, Inc. (2006) Summary page 4.
- K052957: Implantium Prosthetics, Dentium Co., Ltd. (2006) Summary page 4.
- K112045: Simpleline II Abutment System, Dentium Co., Ltd. (2012) Summary page 4.

## Most influential descendants
- K221866: S-Plant Dental Implant System (2024), 2 descendants of its own
- K251605: DIMPLO Implant System (2025), 0 descendants of its own
- K243731: HEXIM Implant; Samwon General Abutments (2025), 0 descendants of its own
- K221847: Ni2 Implant System (2024), 0 descendants of its own
- K231429: S-Plant Dental Implant System (2023), 0 descendants of its own

## Indications for use
Dentium Prosthetics are intended for use as an aid in prosthetic rehabilitation.

Source page: https://510kreport.com/device/K141457
Methodology: https://510kreport.com/methodology