Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3032798406

FEI Number

3032798406

Entity Name

FORG MEDICAL, INC.

City/State/Country

Seattle, WA, US

Establishment Address

13203 39th Ave Ne, Seattle, WA 98125, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

ForG Medical, Inc. (Owner Number: 10091385)

Owner / Operator Contact Address

13203 39th Ave NE, Seattle, WA 98125, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

P-funnel, ONE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NZU	Collector, Urine, Powered, Non Indwelling Catheter	Gastroenterology, Urology	Class 1	876.5250	2024-09-13

Official Correspondent

Daniel Baker

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ForG Medical, 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 3032798406. Last updated year: 2026. Please use registration number 3032798406 when referencing this establishment in official correspondence.