EZPClass II

Rod, Colostomy

21 CFR 876.4270 / Gastroenterology, Urology

EZP is the FDA product code for Rod, Colostomy, a class II device type, regulated under 21 CFR 876.4270. As of 2026-09-10, FDA records hold 2 510(k) clearances under this code, the most recent dated 2006-10-13, and no recalls.

Classification record

Product code: EZP
Device name: Rod, Colostomy
Regulation: 21 CFR 876.4270
Device class: Class II
Review panel: Gastroenterology, Urology
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 2
Ingested recalls: 0

Clearances, product code EZP

By decision year

2 clearances under product code EZP with a decision year between 2004 and 2006, 2004 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code EZP by decision year
Year	Clearances
2004	1
2006	1

Applicants with the most clearances

Product code EZP

Applicants holding the most 510(k) clearances under product code EZP
Applicant	Clearances
MEDLINE INDUSTRIES, LP - Northfield	1
Tools for Surgery, LLC	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 15 companies shown, in name order

Recent clearances

Product code EZP

Recent recalls

Product code EZP

FDA records show no recalls under product code EZP.

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)