# K033644: Endoboy

- Pathway: 510(k) (Traditional)
- Applicant: Geyser S.A.
- Decided: Mar 24, 2004 after 125 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
6 later devices descend from it; 1 cites it directly.
0 of 7 devices 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.

## Most influential descendants
- K071405: Probe Holder System (2007), 5 descendants of its own
- K141523: Ally Ups (2014), 2 descendants of its own
- K223064: ALLY II Uterine Positioning System™ (UPS) (2022), 0 descendants of its own
- K153092: Ally Uterine Positioning System (2015), 0 descendants of its own
- K130758: Kronner Side-Kick Uterine Manipulator Holder (2013), 0 descendants of its own

## Indications for use
The ENDOBOY is a holding and manipulating arm for use in surgery that allows the operating team to hold surgical instruments in a given position and to change that position immediately with one hand

Source page: https://510kreport.com/device/K033644
Methodology: https://510kreport.com/methodology