Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004183707

FEI Number

3004183707

Entity Name

SOLO STEP, INC.

City/State/Country

North Sioux City, SD, US

Establishment Address

610 Freedom Drive Suite 2, North Sioux City, SD 57049, US

Establishment Type(s)

Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

SOLO STEP, INC. (Owner Number: 9103723)

Owner / Operator Contact Address

610 Freedom Drive, Suite 2, North Sioux City, SD 57049, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SOLO-STEP

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IKX	Aid, Transfer	Physical Medicine	Class 1	890.5050	2003-04-30

Official Correspondent

Mike Muth

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SOLO STEP, 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 3004183707. Last updated year: 2026. Please use registration number 3004183707 when referencing this establishment in official correspondence.