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

Applicator, Rapid Wax, Dental

21 CFR 872.3060 / Dental
FDA source (opens on fda.gov)

EIT is the FDA product code for Applicator, Rapid Wax, Dental, a class II device type, regulated under 21 CFR 872.3060. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
EIT
Device name
Applicator, Rapid Wax, Dental
Regulation
21 CFR 872.3060
Device class
Class II
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
1
Ingested recalls
0

Clearances, product code EIT

By decision year
1 clearance under product code EIT with a decision year between 1990 and 1990, 1990 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code EIT by decision year
YearClearances
19901

Applicants with the most clearances

Product code EIT
Applicants holding the most 510(k) clearances under product code EIT
ApplicantClearances
Argen Precious Metals, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code