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

Attachment, Precision, All

21 CFR 872.3165 / Dental
FDA source (opens on fda.gov)

EGG is the FDA product code for Attachment, Precision, All, a class I device type, regulated under 21 CFR 872.3165. As of , FDA records hold 24 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
EGG
Device name
Attachment, Precision, All
Regulation
21 CFR 872.3165
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
24
Ingested recalls
1

Clearances, product code EGG

By decision year
24 clearances under product code EGG with a decision year between 1978 and 1999, 1986 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code EGG by decision year
YearClearances
19781
19791
19811
19821
19831
19841
19864
19872
19881
19892
19903
19912
19921
19941
19961
19991

Applicants with the most clearances

Product code EGG
Applicants holding the most 510(k) clearances under product code EGG
ApplicantClearances
Zest Anchors LLC3
Howmedica Corp.2
Interpore Intl.2
Metalor Dental USA Corp.2
Cogan Corp.1
Cosmetic Dental Technologies, Inc.1
Denta, Inc.1
Dr. Joseph E. Grasso, D.D.S.1
Duradent Corp.1
Gayso Bridge-Tech, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 55 companies shown, in name order