QLINot classified

Vaporizer, Cder Or Cber Led

Unknown

QLI is the FDA product code for Vaporizer, Cder Or Cber Led. FDA's definition for this code reads: "Vaporizers are products that vaporize and deliver drug substance to the site of action through inhalation route". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: QLI
Device name: Vaporizer, Cder Or Cber Led
FDA definition: Vaporizers are products that vaporize and deliver drug substance to the site of action through inhalation route.
Device class: Not classified
Review panel: Unknown
Submission type: Contact ODE
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

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

Recent clearances

Product code QLI

FDA records hold no clearances under product code QLI.

Recent recalls

Product code QLI

FDA records show no recalls under product code QLI.

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)