Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005112128

FEI Number

3005112128

Entity Name

MATSUNAMI GLASS IND.,LTD

City/State/Country

Kishiwada City Osaka, JP

Establishment Address

2-1-10 Yasaka Cho, Kishiwada City Osaka 596-0049, JP

Establishment Type(s)

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

Owner / Operator

Matsunami Glass Ind.,Ltd (Owner Number: 10034688)

Owner / Operator Contact Address

1971 Midway Ste J, Bellingham, WA 98226, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Trubond 380 TOMO MAS MAS-GP APS

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KES	Coverslips, Microscope Slide	Pathology	Class 1	864.3010	2017-01-31
KEW	Slides, Microscope	Pathology	Class 1	864.3010	2010-12-22

Official Correspondent

Takashi Ueda

US Agent Details

Daniel Cybula Business: Matsunami Glass USA Email: Dan.cybula@matsunamiglass.com Phone: (360) 9416911

Related Public Records

Same Entity

Matsunami Glass Ind.,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 3005112128. Last updated year: 2026. Please use registration number 3005112128 when referencing this establishment in official correspondence.