EAHClass I

Cone, Radiographic, Lead-Lined

21 CFR 872.1850 / Dental

EAH is the FDA product code for Cone, Radiographic, Lead-Lined, a class I device type, regulated under 21 CFR 872.1850. As of 2026-09-10, FDA records hold 2 510(k) clearances under this code, the most recent dated 1984-03-16, and no recalls.

Classification record

Product code: EAH
Device name: Cone, Radiographic, Lead-Lined
Regulation: 21 CFR 872.1850
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 EAH

By decision year

2 clearances under product code EAH with a decision year between 1977 and 1984, 1977 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code EAH by decision year
Year	Clearances
1977	1
1984	1

Applicants with the most clearances

Product code EAH

Applicants holding the most 510(k) clearances under product code EAH
Applicant	Clearances
Gary E. Hall, Dds	1
General Electric Co.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code EAH.

Recent clearances

Product code EAH

Recent recalls

Product code EAH

FDA records show no recalls under product code EAH.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)