Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003592318

FEI Number

3003592318

Entity Name

CCB PACKAGING, INC.

City/State/Country

HIAWATHA, IA, US

Establishment Address

1905 NORTH CENTER POINT RD., HIAWATHA, IA 52233, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

CCB Packaging, Inc. (Owner Number: 9047401)

Owner / Operator Contact Address

1905 NORTH CENTER POINT RD., --, Hiawatha, IA 52233, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

DEN220078

PMA Number

N/A

All Registered Proprietary Names

Eroxon

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HIS	Condom	Obstetrics/Gynecology	Class 2	884.5300	2022-08-18
MOL	Condom, Synthetic	Obstetrics/Gynecology	Class 2	884.5300	2022-08-18
LTZ	Condom With Nonoxynol-9	Obstetrics/Gynecology	Class 2	884.5310	2022-08-18
HIS	Condom	Obstetrics/Gynecology	Class 2	884.5300	2022-08-18
HIS	Condom	Obstetrics/Gynecology	Class 2	884.5300	2022-08-18
QWW	Non-Medicated Topical Formulation For Treatment Of Erectile Dysfunction.	Gastroenterology, Urology	Class 2	876.5021	2024-10-28

Official Correspondent

Matt Weber

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CCB Packaging, 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 3003592318. Last updated year: 2026. Please use registration number 3003592318 when referencing this establishment in official correspondence.