LNQHumanitarian device exemption

Intestinal Stimulator

Unknown

LNQ is the FDA product code for Intestinal Stimulator. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code: LNQ
Device name: Intestinal Stimulator
Device class: Humanitarian device exemption
Review panel: Unknown
Submission type: FDA code 6
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 1

Companies listing this code with FDA

Companies whose registered establishments list this code

Recent clearances

Product code LNQ

FDA records hold no clearances under product code LNQ.

Recent recalls

Product code LNQ

Z-0088-2010Medtronic is in the process of updating the Enterra Therapy labeling to include information regarding the risks of bowel...Medtronic Neuromodulation / initiated 2009-08-25 / 1909 (1095 US, 814 OUS)

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)