# K141523: Ally Ups

- Pathway: 510(k) (Traditional)
- Applicant: CooperSurgical, Inc.
- Decided: Nov 25, 2014 after 169 days
- Product code: LKF (Cannula, Manipulator/Injector, Uterine)
- Device class: 2
- Regulation: 21 CFR 884.4530
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K941458 (1995). 3 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071405: Probe Holder System, Intuitive Surgical, Inc. (2007) Summary page 5.

## Most influential descendants
- K223064: ALLY II Uterine Positioning System™ (UPS) (2022), 0 descendants of its own
- K153092: Ally Uterine Positioning System (2015), 0 descendants of its own

## Recalls of this device
- May 18, 2015 · Class II · Z-1727-2015: Design of device may expose user to injury to fingers or body parts

## Indications for use
The Ally Uterine Positioning System™ (Ally UPS) is intended to assist the surgical staff in mounting, positioning, and holding uterine manipulators during gynecological laparoscopic procedures. It is intended for use by trained operating room personnel in an operating room environment. The Adapter Drape for the Ally Uterine Positioning System™ (Ally UPS) is intended to assist the surgical staff in mounting, positioning, and holding uterine manipulators during gynecological laparoscopic procedures. It is intended for use by trained operating room personnel in an operating room environment.

Source page: https://510kreport.com/device/K141523
Methodology: https://510kreport.com/methodology