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

Disk, Abrasive

21 CFR 872.6010 / Dental
FDA source (opens on fda.gov)

EHJ is the FDA product code for Disk, Abrasive, a class I device type, regulated under 21 CFR 872.6010. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
EHJ
Device name
Disk, Abrasive
Regulation
21 CFR 872.6010
Device class
Class I
Review panel
Dental
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
4
Ingested recalls
2

Clearances, product code EHJ

By decision year
4 clearances under product code EHJ with a decision year between 1977 and 1991, 1977 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code EHJ by decision year
YearClearances
19771
19791
19871
19911

Applicants with the most clearances

Product code EHJ
Applicants holding the most 510(k) clearances under product code EHJ
ApplicantClearances
Cavitron Corp.1
Centrix, Inc.1
E.C. Moore Co.1
Vermont Diamond Instruments1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 87 companies shown, in name order