# K102769: Neodent Implant for Orthodontic Anchorage

- Pathway: 510(k) (Traditional)
- Applicant: Jjgc Industria E Comercio DE Materiais Dentarios S
- Decided: Feb 23, 2011 after 152 days
- Product code: OAT (Implant, Endosseous, Orthodontic)
- 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: 9 generations back to K894844 (1990). 25 ancestors in all.
No later device cites it as a predicate yet.
0 of 26 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082838: Orlus Mini Screw, Ortholution Co., Ltd. (2008) Summary page 2.
- K041527: Aarhus Anchorage System, Medicon EG (2004) Summary page 2.
- K090476: Syntec Orthodontic Mini Screw, Syntec Scientific Corp. (2009) Summary page 2.

## Indications for use
This product is a surgical device in the form of a temporary screw used as an aid in orthodontic movement procedures.

Source page: https://510kreport.com/device/K102769
Methodology: https://510kreport.com/methodology