Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017968993

FEI Number

3017968993

Entity Name

ENDOSOUND INC

City/State/Country

Portland, OR, US

Establishment Address

4640 S Macadam Ave, Ste 200, Portland, OR 97239, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

EndoSound Inc (Owner Number: 10089762)

Owner / Operator Contact Address

4640 S Macadam Ave, Ste 200, Portland, OR 97239, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Air Leakage Tester

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FCY	Bulb, Inflation, For Endoscope	Gastroenterology, Urology	Class 1	876.1500	2024-01-18

Official Correspondent

Patrick Herriman

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

EndoSound 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 3017968993. Last updated year: 2026. Please use registration number 3017968993 when referencing this establishment in official correspondence.