Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3018783049

FEI Number

3018783049

Entity Name

CONTINENTAL LOGISTICS SOLUTIONS, INC.

City/State/Country

Elk Grove Village, IL, US

Establishment Address

2881 N. Busse Road, Elk Grove Village, IL 60007, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Continental Logistics Solutions, Inc. (Owner Number: 10081519)

Owner / Operator Contact Address

2881 N. Busse Road, Elk Grove Village, IL 60007, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HHE	Cup, Menstrual	Obstetrics/Gynecology	Class 2	884.5400	2021-04-21

Official Correspondent

Steve Johnson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Continental Logistics Solutions, 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 3018783049. Last updated year: 2026. Please use registration number 3018783049 when referencing this establishment in official correspondence.