QUNClass II

Tether Accessory For Use In The Gastrointestinal Tract

21 CFR 876.1305 / Gastroenterology, Urology

QUN is the FDA product code for Tether Accessory For Use In The Gastrointestinal Tract, a class II device type, regulated under 21 CFR 876.1305. FDA's definition for this code reads: "A non-powered, detachable, flexible tether accessory used to maneuver a swallowed device, such as a capsule, in the upper gastrointestinal tract". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: QUN
Device name: Tether Accessory For Use In The Gastrointestinal Tract
FDA definition: A non-powered, detachable, flexible tether accessory used to maneuver a swallowed device, such as a capsule, in the upper gastrointestinal tract.
Regulation: 21 CFR 876.1305
Device class: Class II
Review panel: Gastroenterology, Urology
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 0

Companies listing this code with FDA

Companies whose registered establishments list this code

Anx Robotica Corp.

Recent clearances

Product code QUN

FDA records hold no clearances under product code QUN.

Recent recalls

Product code QUN

FDA records show no recalls under product code QUN.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)