510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
EHEClass I

Dispenser, Mercury And/Or Alloy

21 CFR 872.3080 / Dental
FDA source (opens on fda.gov)

EHE is the FDA product code for Dispenser, Mercury And/Or Alloy, a class I device type, regulated under 21 CFR 872.3080. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
EHE
Device name
Dispenser, Mercury And/Or Alloy
Regulation
21 CFR 872.3080
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
2
Ingested recalls
0

Clearances, product code EHE

By decision year
2 clearances under product code EHE with a decision year between 1977 and 1977, 1977 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code EHE by decision year
YearClearances
19772

Applicants with the most clearances

Product code EHE
Applicants holding the most 510(k) clearances under product code EHE
ApplicantClearances
Johnson & Johnson Professionals, Inc.1
New Dimensions in Medicine, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code