PARO ROBOTS U.S. INC.

FDA Device Registration & Listing · Itasca, IL, US · Registration 3009118691

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
3009118691
FEI Number
3009118691
Entity Name
PARO ROBOTS U.S. INC.
City/State/Country
Itasca, IL, US
Establishment Address
150 E Pierce Rd Suite 550, Itasca, IL 60143, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
PARO Robots U.S. Inc. (Owner Number: 10041171)
Owner / Operator Contact Address
150 E Pierce Road, Suite 550, Itasca, IL 60143, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Paro Robots

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HCC Device, Biofeedback Neurology Class 2 882.5050 2012-06-27

Official Correspondent

Shinichiro Kishioka

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PARO Robots U.S. Inc.
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
K873418 Bodylog, Inc. BODYLOG STRESS REDUCTION PACKAGE 1987-12-17
K792659 Bio-Feedback Systems, Inc. FEEDBACK EDR SYSTEM MODEL ME-1 1980-01-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009118691. Last updated year: 2026. Please use registration number 3009118691 when referencing this establishment in official correspondence.
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