Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3025300237

FEI Number

3025300237

Entity Name

HOPE MEDICAL

City/State/Country

Grayslake, IL, US

Establishment Address

888 E Belvidere Rd Ste 212, Grayslake, IL 60030, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Hope Medical (Owner Number: 10086687)

Owner / Operator Contact Address

888 E Belvidere Road, Suite 212, Grayslake, IL 60030, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Infinity Balloon Dilation Catheter

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KCF	Dilator, Esophageal, Ent	Ear, Nose, Throat	Class 1	874.4420	2022-12-02

Official Correspondent

Paul Imaoka

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Hope Medical

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 3025300237. Last updated year: 2026. Please use registration number 3025300237 when referencing this establishment in official correspondence.