Mochida Pharmaceutical Co., Ltd. Fujieda site

FDA Device Registration & Listing · Fujieda Shizuoka, JP · Registration 3015380522

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
3015380522
FEI Number
3015380522
Entity Name
Mochida Pharmaceutical Co., Ltd. Fujieda site
City/State/Country
Fujieda Shizuoka, JP
Establishment Address
342 Gensuke, Fujieda Shizuoka 4268640, JP
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Mochida Pharmaceutical Co., LTD (Owner Number: 10091242)
Owner / Operator Contact Address
1-7, Yotsuya, Shinjuku-ku, JP-13 1608515, JP
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K233322
PMA Number
N/A

All Registered Proprietary Names

ReFeel

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JXI Cuff, Nerve Neurology Class 2 882.5275 2024-08-28

Official Correspondent

No official correspondent registered.

US Agent Details

Keith Barritt Business: Fish & Richardson P.C. Email: barritt@fr.com Phone: (202) 6266433

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
9612125 MOCHIDA PHARMACEUTICAL CO., LTD Shinjuku-ku Tokyo, JP

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015380522. Last updated year: 2026. Please use registration number 3015380522 when referencing this establishment in official correspondence.
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