# K140091: Xpeed Anyridge Internal Implant Sysyem

- Pathway: 510(k) (Traditional)
- Applicant: Megagen Implant Co., Ltd.
- Decided: Dec 12, 2014 after 332 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.
9 later devices descend from it; 2 cite it directly.
0 of 80 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 6.
- K061176: Straumann Dental Implants, Institut Straumann AG (2006) Summary page 6.

## Most influential descendants
- K170044: Inclusive Titanium Abutments compatible with: MegaGen AnyRidge Implant System (2017), 5 descendants of its own
- K191222: Inclusive Titanium Abutments compatible with: Dentsply Implants Astra Tech Implant System EV (2019), 4 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
- K253334: ZENEX Implant System_Short (R-System) (2026), 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 fully edentulous individuals. It is used to restore a patient’s chewing function. Smaller implants (less than Ø6.0 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/K140091
Methodology: https://510kreport.com/methodology