Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015422018

FEI Number

3015422018

Entity Name

VOXAPOD, INC

City/State/Country

Portland, OR, US

Establishment Address

8518 NW Gilliam Lane, Portland, OR 97229, US

Establishment Type(s)

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

Owner / Operator

VOXAPOD, Inc (Owner Number: 10059946)

Owner / Operator Contact Address

901 SW King Ave, 12D, Portland, OR 97205, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

VOXAPOD

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HHE	Cup, Menstrual	Obstetrics/Gynecology	Class 2	884.5400	2019-03-13

Official Correspondent

Amanda Wilson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

VOXAPOD, 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 3015422018. Last updated year: 2026. Please use registration number 3015422018 when referencing this establishment in official correspondence.