Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007617202

FEI Number

3007617202

Entity Name

Commercial Plastics

City/State/Country

Kenosha, WI, US

Establishment Address

9600 55th St, Kenosha, WI 53144, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Commercial Plastics (Owner Number: 10027917)

Owner / Operator Contact Address

9600 55th street, Kenosha, WI 53144, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Sharps Container Sharps Container Sharps Container

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MMK	Container, Sharps	General Hospital	Class 2	880.5570	2008-12-15
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2008-12-15
MMK	Container, Sharps	General Hospital	Class 2	880.5570	2008-12-15
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2008-12-15
MMK	Container, Sharps	General Hospital	Class 2	880.5570	2014-03-19

Official Correspondent

Cary Brown

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Commercial Plastics

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K812404	Nu Tech Medical Systems	BUTTERFLY NEEDLE ASSEMBLY	1981-09-09

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0002-2022	Bard Peripheral Vascular Inc	2	REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796

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3007097064	STERICYCLE, INC.	Bannockburn, IL, US
3013557562	CBR ENTERPRISE LIMITED	Hong Kong, HK

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007617202. Last updated year: 2026. Please use registration number 3007617202 when referencing this establishment in official correspondence.