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

Bar, Preformed

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

EHO is the FDA product code for Bar, Preformed, a class I device type, regulated under 21 CFR 872.3165. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
EHO
Device name
Bar, Preformed
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
3
Ingested recalls
0

Clearances, product code EHO

By decision year
3 clearances under product code EHO with a decision year between 1988 and 1994, 1988 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code EHO by decision year
YearClearances
19881
19891
19941

Applicants with the most clearances

Product code EHO
Applicants holding the most 510(k) clearances under product code EHO
ApplicantClearances
Dale T. Dupuis1
Gatewood Splints1
Trophy Radiologie1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 27 companies shown, in name order