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

Wire, Orthodontic

21 CFR 872.5410 / Dental
FDA source (opens on fda.gov)

DZC is the FDA product code for Wire, Orthodontic, a class I device type, regulated under 21 CFR 872.5410. As of , FDA records hold 30 510(k) clearances under this code, the most recent dated , and 4 recalls.

Classification record

Product code
DZC
Device name
Wire, Orthodontic
Regulation
21 CFR 872.5410
Device class
Class I
Review panel
Dental
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
30
Ingested recalls
4

Clearances, product code DZC

By decision year
30 clearances under product code DZC with a decision year between 1981 and 2011, 1993 the highest year at 10.
Show the numbers
510(k) clearances under FDA product code DZC by decision year
YearClearances
19811
19844
19853
19861
19925
199310
19945
20111

Applicants with the most clearances

Product code DZC
Applicants holding the most 510(k) clearances under product code DZC
ApplicantClearances
G & H Wire Company7
Ultimate Wireforms, Inc.5
Gac Intl., Inc.3
Berkley and Co.2
Dentauraum, Inc.2
Flexmedics2
A Company, Inc.1
A Company, Inc.1
Albert J. Anthony, Dmd1
Arthur L. Wool1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 167 companies shown, in name order