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

Elevator, Surgical, Dental

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

EMJ is the FDA product code for Elevator, Surgical, Dental, a class I device type, regulated under 21 CFR 872.4565. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
EMJ
Device name
Elevator, Surgical, 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
6
Ingested recalls
0

Clearances, product code EMJ

By decision year
6 clearances under product code EMJ with a decision year between 1977 and 1987, 1985 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code EMJ by decision year
YearClearances
19771
19821
19853
19871

Applicants with the most clearances

Product code EMJ
Applicants holding the most 510(k) clearances under product code EMJ
ApplicantClearances
Artiberia2
Depuy, Inc.1
Ipco Corp.1
Military Engineering, Inc.1
Pacific Dental Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 231 companies shown, in name order