# K042171: Ax's Endo 04, 06, 08, 2.5, 40 , Models 50100206, 50100217, 50100218, 50100230, 50100232

- Pathway: 510(k) (Traditional)
- Applicant: Micro-Mega Societe Anonyme
- Decided: Nov 10, 2004 after 91 days
- Product code: EGS (Handpiece, Contra- And Right-Angle Attachment, Dental)
- Device class: 1
- Regulation: 21 CFR 872.4200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
Ax's Endo® handpieces are intended to hold burs or other tools and to transmit rotational movement to these via a motor.

Source page: https://510kreport.com/device/K042171
Methodology: https://510kreport.com/methodology