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

Drill, Dental, Intraoral

21 CFR 872.4130 / Dental
FDA source (opens on fda.gov)

DZA is the FDA product code for Drill, Dental, Intraoral, a class I device type, regulated under 21 CFR 872.4130. As of , FDA records hold 13 510(k) clearances under this code, the most recent dated , and 3 recalls.

Classification record

Product code
DZA
Device name
Drill, Dental, Intraoral
Regulation
21 CFR 872.4130
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
13
Ingested recalls
3

Clearances, product code DZA

By decision year
13 clearances under product code DZA with a decision year between 1976 and 1999, 1976 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code DZA by decision year
YearClearances
19762
19802
19811
19881
19902
19911
19931
19962
19991

Applicants with the most clearances

Product code DZA
Applicants holding the most 510(k) clearances under product code DZA
ApplicantClearances
Aesculap Instruments Corp.2
Allomedic1
American Safety Equipment Corp.1
Del Medical Systems Corp.1
Dentsply Intl.1
Implant Corp. of America1
Ivoclar North America, Inc.1
Phillip C. Crawford, D.D.S.1
Signature One Products, Inc.1
The Hygenic Company, LLC1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 181 companies shown, in name order