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

Anchor, Preformed

21 CFR 872.3130 / Dental
FDA source (opens on fda.gov)

EJX is the FDA product code for Anchor, Preformed, a class I device type, regulated under 21 CFR 872.3130. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
EJX
Device name
Anchor, Preformed
Regulation
21 CFR 872.3130
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
1
Ingested recalls
0

Clearances, product code EJX

By decision year
1 clearance under product code EJX with a decision year between 2015 and 2015, 2015 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code EJX by decision year
YearClearances
20151

Applicants with the most clearances

Product code EJX
Applicants holding the most 510(k) clearances under product code EJX
ApplicantClearances
M&M Dental Studio, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 16 companies shown, in name order