510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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EGZClass I

Holder, Film, X-Ray

21 CFR 872.1905 / Dental
FDA source (opens on fda.gov)

EGZ is the FDA product code for Holder, Film, X-Ray, a class I device type, regulated under 21 CFR 872.1905. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
EGZ
Device name
Holder, Film, X-Ray
Regulation
21 CFR 872.1905
Device class
Class I
Review panel
Dental
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
8
Ingested recalls
0

Clearances, product code EGZ

By decision year
8 clearances under product code EGZ with a decision year between 1980 and 1991, 1985 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code EGZ by decision year
YearClearances
19801
19821
19852
19861
19891
19912

Applicants with the most clearances

Product code EGZ
Applicants holding the most 510(k) clearances under product code EGZ
ApplicantClearances
Nix Co., Ltd.2
Bite-A-Block1
Henry Schein, Inc.1
Rinn Corp.1
Strong Marketing1
The S. S. White Co.1
Trollplast, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 127 companies shown, in name order