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

Light, Fiber Optic, Dental

21 CFR 872.4620 / Dental
FDA source (opens on fda.gov)

EAY is the FDA product code for Light, Fiber Optic, Dental, a class I device type, regulated under 21 CFR 872.4620. As of , FDA records hold 18 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
EAY
Device name
Light, Fiber Optic, Dental
Regulation
21 CFR 872.4620
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
18
Ingested recalls
0

Clearances, product code EAY

By decision year
18 clearances under product code EAY with a decision year between 1976 and 1995, 1980 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code EAY by decision year
YearClearances
19762
19771
19781
19792
19804
19811
19821
19832
19871
19941
19952

Applicants with the most clearances

Product code EAY
Applicants holding the most 510(k) clearances under product code EAY
ApplicantClearances
Midwest5
Beaverstate Dental, Inc.2
Lares Manufacturing Co., Inc.2
Chayes Virginia, Inc.1
Den-Mat Corp.1
Jedental Co., Inc.1
Ritter GmbH1
Silverman'S1
Stryker Corp.1
Syntex Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 24 companies shown, in name order