# K123870: Xpeed Anyridge Internal Implant System

- Pathway: 510(k) (Special)
- Applicant: Megagen Implant Co., Ltd.
- Decided: Mar 27, 2013 after 100 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: 10 generations back to K944964 (1995). 71 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 73 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070562: EZ Plus Implant System, Megagen Co., Ltd. (2007) Summary page 2.
- K122231: Xpeed Any Ridge Internal Implant System, Megagen Implant Co., Ltd. (2012) Summary page 2.

## Most influential descendants
- K242261: Accelx Implant System (2024), 0 descendants of its own

## Indications for use
The Xpeed® AnyRidge® Internal Implant System is intended to be surgically placed in the maxillary or mandibular molar areas for the purpose providing prosthetic support for dental restorations(Crown, bridges, and overdentures) in partially or Bfilly edentulous individuals. It is used to restore a patient's chewing funiction. Smaller implants (less than 06.0mm) are dedicated for immediate loading when good primary stability is achieved and with appropriate occlusal loading. Larger implants are dedicated for the molar region and are indicated for delayed loading.

Source page: https://510kreport.com/device/K123870
Methodology: https://510kreport.com/methodology