# K050926: Texan Longhorn Foreign Body Retrieval Device, Model TX30120060

- Pathway: 510(k) (Special)
- Applicant: Idev Technologies, Inc.
- Decided: May 9, 2005 after 26 days
- Product code: MMX (Device, Percutaneous Retrieval)
- Device class: 2
- Regulation: 21 CFR 870.5150
- 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. The FDA summary names its predicate without a number.
- (no number) Texan™ Foreign Body Retrieval Device: named in the summary without a submission number

## Indications for use
The Texan LONGhornTM Foreign Body Retrieval Device is intended for use as a tool to retrieve and manipulate foreign bodies from distal peripheral vessels of the cardiovascular system.

Source page: https://510kreport.com/device/K050926
Methodology: https://510kreport.com/methodology