MEDIVR.INC

FDA Device Registration & Listing · Toyonaka Osaka, JP · Registration 3022516898

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
3022516898
FEI Number
3022516898
Entity Name
MEDIVR.INC
City/State/Country
Toyonaka Osaka, JP
Establishment Address
Ryokuchieki Bld 3F. VRzigyoubumon, 2-4-1, Toyonaka Osaka 561-0872, JP
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Remanufacture Medical Device,Manufacture Medical Device
Owner / Operator
mediVR.Inc (Owner Number: 10084971)
Owner / Operator Contact Address
2-3-8 Terauchi, Toyonaka, JP-27 561-0872, JP
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

mediVR KAGURA

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ISD Exerciser, Measuring Physical Medicine Class 2 890.5360 2022-04-21

Official Correspondent

Masahiko Hara

US Agent Details

Takahiro Haruyama Email: register@globizz.net Phone: (310) 5383860

Related Public Records

Same Entity

mediVR.Inc
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 3022516898. Last updated year: 2026. Please use registration number 3022516898 when referencing this establishment in official correspondence.
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