Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3039644422

FEI Number

3039644422

Entity Name

EzaLife Inc.

City/State/Country

Aurora, CO, US

Establishment Address

12635 E Montview Blvd Ste 100, Aurora, CO 80045, US

Establishment Type(s)

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

Owner / Operator

Ezalife LLC (Owner Number: 10093926)

Owner / Operator Contact Address

12635 E Montview Blvd Ste 100, Aurora, CO 80045, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Button Huggie

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PLI	Gastrointestional Tube Holder	Gastroenterology, Urology	Class 2	876.5980	2025-08-07

Official Correspondent

Bryan Norman

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Ezalife LLC

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 3039644422. Last updated year: 2026. Please use registration number 3039644422 when referencing this establishment in official correspondence.