Yoshikawa Kasei Co., Ltd. Medical Company Shizuoka Plant

FDA Device Registration & Listing · Fukuroi City Shizuoka, JP · Registration 3014055212

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
3014055212
FEI Number
3014055212
Entity Name
Yoshikawa Kasei Co., Ltd. Medical Company Shizuoka Plant
City/State/Country
Fukuroi City Shizuoka, JP
Establishment Address
1217-12 Tomonaga, Fukuroi City Shizuoka 437-0004, JP
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
MIC International (Owner Number: 10087043)
Owner / Operator Contact Address
201 E 69th Street, Suite 5O, New York, NY 10021, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PEA Endoscope, Accessories, Image Post-Processing For Color Enhancement Gastroenterology, Urology Class 2 876.1500 2023-01-05
EOB Nasopharyngoscope (Flexible Or Rigid) Ear, Nose, Throat Class 2 874.4760 2023-01-05
FDT Duodenoscope And Accessories, Flexible/Rigid Gastroenterology, Urology Class 2 876.1500 2023-01-05

Official Correspondent

Deno Zachary

US Agent Details

Deno Zachary Business: MIC International Email: dzachary@micinternational.com Phone: (917) 3315789

Related Public Records

Same Entity

MIC International
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3004638277 Yoshikawa Kasei Co., Ltd. Medical Company Osaka Plant Osaka-shi, JP

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K220587 Olympus Medical Systems Corp. Evis Exera III Duodenovideoscope Olympus TJF-Q190V 2022-05-11

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014055212. Last updated year: 2026. Please use registration number 3014055212 when referencing this establishment in official correspondence.
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