Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3038914432

FEI Number

3038914432

Entity Name

AUGGIE, INC.

City/State/Country

Denver, CO, US

Establishment Address

4508 Lowell Blvd, Denver, CO 80211, US

Establishment Type(s)

Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Auggie, Inc. (Owner Number: 10093171)

Owner / Operator Contact Address

4383 Tennyson St, Unit 3i, Denver, CO 80212, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Auggie Breast Implant Sizer

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NOJ	Prosthesis, Breast, External, No Adhesive	General, Plastic Surgery	Class 1	878.3800	2025-06-04

Official Correspondent

Ashleigh DePopas

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Auggie, 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 3038914432. Last updated year: 2026. Please use registration number 3038914432 when referencing this establishment in official correspondence.