EZZClass III

Prosthesis, Vas Deferens

Unknown

EZZ is the FDA product code for Prosthesis, Vas Deferens, a class III device type. As of 2026-09-10, FDA records hold one 510(k) clearance under this code, the most recent dated 1985-07-02, and no recalls.

Classification record

Product code: EZZ
Device name: Prosthesis, Vas Deferens
Device class: Class III
Review panel: Unknown
Submission type: PMA
Implant: Yes
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 1
Ingested recalls: 0

Clearances, product code EZZ

By decision year

1 clearance under product code EZZ with a decision year between 1985 and 1985, 1985 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code EZZ by decision year
Year	Clearances
1985	1

Applicants with the most clearances

Product code EZZ

Applicants holding the most 510(k) clearances under product code EZZ
Applicant	Clearances
Artiberia	1

Companies listing this code with FDA

Companies whose registered establishments list this code

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

Recent clearances

Product code EZZ

K851719Class III1070/15 to 1078/17 Various Types Needle HoldersArtiberia / cleared 1985-07-02

Recent recalls

Product code EZZ

FDA records show no recalls under product code EZZ.

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)