Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006606966

FEI Number

3006606966

Entity Name

J. MORITA CORP.

City/State/Country

TARUMI-CHO Osaka, JP

Establishment Address

33-18, 3 CHOME, TARUMI-CHO Osaka 564-8650, JP

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

J. MORITA USA (Owner Number: 8030247)

Owner / Operator Contact Address

9 Mason, Irvine, CA 92618, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Amalgam Carver MORITA DISPOSABLE DENTAL NEEDLE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EKH	Carver, Dental Amalgam, Operative	Dental	Class 1	872.4565	2009-08-12
DZM	Needle, Dental	Dental	Class 1	872.4730	1998-03-06

Official Correspondent

No official correspondent registered.

US Agent Details

Keith Barritt Business: FISH & RICHARDSON P.C. Email: barritt@fr.com Phone: (202) 7835070

Related Public Records

Same Entity

J. MORITA USA

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
2081055	J. MORITA USA, INC.	IRVINE, CA, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006606966. Last updated year: 2026. Please use registration number 3006606966 when referencing this establishment in official correspondence.