ISHIDA MEDICAL LLC

FDA Device Registration & Listing · Irvine, CA, US · Registration 3023229466

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
3023229466
FEI Number
3023229466
Entity Name
ISHIDA MEDICAL LLC
City/State/Country
Irvine, CA, US
Establishment Address
5151 Califorinia Ave #100, Irvine, CA 92617, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
ISHIDA MEDICAL LLC (Owner Number: 10085610)
Owner / Operator Contact Address
5151 Califorinia Ave #100, Irvine, CA 92617, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Uro Checker Hemato Check Module

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EXR Urinometer, Mechanical Gastroenterology, Urology Class 2 876.1800 2022-07-10
CDM Diazonium Colorimetry, Urobilinogen (Urinary, Non-Quant.) Clinical Chemistry Class 1 862.1785 2022-07-10

Official Correspondent

Makoto Nakatani

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ISHIDA MEDICAL LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3023229466. Last updated year: 2026. Please use registration number 3023229466 when referencing this establishment in official correspondence.
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