DNXClass II

Lead, Protoporphyrin Zinc Method, Fluorometric

21 CFR 862.3550 / Clinical Toxicology

DNX is the FDA product code for Lead, Protoporphyrin Zinc Method, Fluorometric, a class II device type, regulated under 21 CFR 862.3550. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: DNX
Device name: Lead, Protoporphyrin Zinc Method, Fluorometric
Regulation: 21 CFR 862.3550
Device class: Class II
Review panel: Clinical Toxicology
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

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

Recent clearances

Product code DNX

FDA records hold no clearances under product code DNX.

Recent recalls

Product code DNX

FDA records show no recalls under product code DNX.

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)