Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1824299

FEI Number

1824299

Entity Name

E. C. MOORE COMPANY, INC.

City/State/Country

Dearborn, MI, US

Establishment Address

13325 Leonard Street, Dearborn, MI 48126, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

E. C. Moore Company, Inc. (Owner Number: 10031306)

Owner / Operator Contact Address

13325 Leonard Street, Dearborn, MI 48126, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

E.C. Moore PopWhite Prophy Paste E.C. Moore; Cosmedenr

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EHL	Point, Abrasive	Dental	Class 1	872.6010	2013-03-25
EJR	Agent, Polishing, Abrasive, Oral Cavity	Dental	Class 1	872.6030	2010-01-22
EHJ	Disk, Abrasive	Dental	Class 1	872.6010	2010-01-14

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

E. C. Moore Company, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K121698	Dentsply International, Inc.	NUPRO SENSODYNE PROPHYLAXIS PASTE WITH NOVAMIN	2012-08-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1824299. Last updated year: 2026. Please use registration number 1824299 when referencing this establishment in official correspondence.