# K122231: Xpeed Any Ridge Internal Implant System

- Pathway: 510(k) (Special)
- Applicant: Megagen Implant Co., Ltd.
- Decided: Oct 4, 2012 after 70 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: 9 generations back to K944964 (1995). 70 ancestors in all.
25 later devices descend from it; 5 cite it directly.
0 of 96 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K110955: Anyridge Internal Implant System, Megagen Co., Ltd. (2011) Summary page 2.
- K061176: Straumann Dental Implants, Institut Straumann AG (2006) Summary page 2.

## Most influential descendants
- K123988: Anyonetm Internal Implant System (2013), 19 descendants of its own
- K182448: AnyRidge Octa 1 Implant System (2019), 9 descendants of its own
- K200817: URIS OMNI Narrow System & Prosthetic (2020), 6 descendants of its own
- K203240: AccelX Abutments (2021), 2 descendants of its own
- K252585: ZENEX Implant System_R-System (2026), 1 descendant 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 fully edentulous individuals. It is used to restore a patient's chewing function. Smaller implants (less than 06.0 mm) 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/K122231
Methodology: https://510kreport.com/methodology