MORITA ELECTRIC MFG., LTD.

FDA Device Registration & Listing · HIKONE Shiga, JP · Registration 8043608

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
8043608
FEI Number
3010325304
Entity Name
MORITA ELECTRIC MFG., LTD.
City/State/Country
HIKONE Shiga, JP
Establishment Address
1395 TAKAMIYA-CHO, HIKONE Shiga 522-0201, JP
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
MORITA ELECTRIC MFG., LTD. (Owner Number: 9002641)
Owner / Operator Contact Address
1395 TAKAMIYA-CHO, --, HIKONE, JP-25 --, JP
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Surgical Clipper

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LWK Razor, Surgical General, Plastic Surgery Class 1 878.4800 1991-11-07

Official Correspondent

SATIO BANDO

US Agent Details

Tom Juliano Email: Tom.Juliano@us.panasonic.com Phone: (201) 3487758

Related Public Records

Same Entity

MORITA ELECTRIC MFG., LTD.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8043608. Last updated year: 2026. Please use registration number 8043608 when referencing this establishment in official correspondence.
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