FUJIFILM ashigara factory

FDA Device Registration & Listing · Kanagawa, JP · Registration 3008770689

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
3008770689
FEI Number
3008770689
Entity Name
FUJIFILM ashigara factory
City/State/Country
Kanagawa, JP
Establishment Address
210 Nakanuma, Minami, Minami-Ashigara, Kanagawa 250-0193, JP
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
FUJIFILM Holdings Corporation (Owner Number: 10034608)
Owner / Operator Contact Address
7-3, Akasaka 9-chome, Minato-ku, Tokyo, JP-13 107-0052, JP
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Tissue-Tek Coverslipping Film

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KES Coverslips, Microscope Slide Pathology Class 1 864.3010 2010-12-15

Official Correspondent

No official correspondent registered.

US Agent Details

Solmaz M Shaida Business: Sakura Finetek USA Email: sshaida@sakuraus.com Phone: (310) 7835076

Related Public Records

Same Entity

FUJIFILM Holdings Corporation
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 3008770689. Last updated year: 2026. Please use registration number 3008770689 when referencing this establishment in official correspondence.
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