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

Carver, Wax, Dental

21 CFR 872.4565 / Dental
FDA source (opens on fda.gov)

EIK is the FDA product code for Carver, Wax, Dental, a class I device type, regulated under 21 CFR 872.4565. As of , FDA records hold 5 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
EIK
Device name
Carver, Wax, Dental
Regulation
21 CFR 872.4565
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
5
Ingested recalls
0

Clearances, product code EIK

By decision year
5 clearances under product code EIK with a decision year between 1985 and 2002, 1985 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code EIK by decision year
YearClearances
19851
19861
19901
19981
20021

Applicants with the most clearances

Product code EIK
Applicants holding the most 510(k) clearances under product code EIK
ApplicantClearances
Artiberia1
Estrad B.V.1
Intl. Equipment and Supply Corp.1
Pacific Union Dental, Inc.1
Stephen M Koral, Dmd1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 102 companies shown, in name order