Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3038008627

FEI Number

3038008627

Entity Name

FILLOW INC.

City/State/Country

Northbrook, IL, US

Establishment Address

666 Dundee Rd Ste 1703, Northbrook, IL 60062, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Fillow Inc. (Owner Number: 10092897)

Owner / Operator Contact Address

666 Dundee Road, Suite 1703, Northbrook, IL 60062, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Fillow Disc & Applicator

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HHE	Cup, Menstrual	Obstetrics/Gynecology	Class 2	884.5400	2025-04-07

Official Correspondent

Heekyoung Woo

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Fillow 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 3038008627. Last updated year: 2026. Please use registration number 3038008627 when referencing this establishment in official correspondence.