MQONot classified

Prosthetic Disc Nucleus Device

Unknown

MQO is the FDA product code for Prosthetic Disc Nucleus Device. FDA's definition for this code reads: "Export only". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: MQO
Device name: Prosthetic Disc Nucleus Device
FDA definition: Export only
Device class: Not classified
Review panel: Unknown
Submission type: Contact ODE
Implant: Yes
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

No registered establishment in MDM’s records lists product code MQO.

Recent clearances

Product code MQO

FDA records hold no clearances under product code MQO.

Recent recalls

Product code MQO

FDA records show no recalls under product code MQO.

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)