DIA PHARMACEUTICAL CO., LTD

FDA Device Registration & Listing · Kashihara Nara, JP · Registration 3010045207

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
3010045207
FEI Number
3010045207
Entity Name
DIA PHARMACEUTICAL CO., LTD
City/State/Country
Kashihara Nara, JP
Establishment Address
515 Jyobonji-cho, Kashihara Nara 6340803, JP
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
DIA Pharmaceutical Co., Ltd (Owner Number: 10044221)
Owner / Operator Contact Address
515 Jyobonji-cho, Kashihara, JP-29 6340803, JP
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Stona Cooling Gel Pads

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IMD Pack, Hot Or Cold, Disposable Physical Medicine Class 1 890.5710 2013-05-14

Official Correspondent

Daizo Morikane

US Agent Details

Yasumi Goyal Business: DIA Pharmaceutical Co., Ltd Email: overseas-reg@dia-pharma.com Phone: (424) 2148301

Related Public Records

Same Entity

DIA Pharmaceutical Co., Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K880871 John Wagner Associates, Inc. GRABBER WARM PACK/MINI MINI HEATER/FOOT HEATER 1988-05-20

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0505-2022 Philips North America Llc 1
Infa-Therm Transport Mattress, Reference Number 989805616831 1015
Z-0506-2022 Philips North America Llc 1
Infant Heel Warmers w/strap, Reference # 989805603201 1223

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010045207. Last updated year: 2026. Please use registration number 3010045207 when referencing this establishment in official correspondence.
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