Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007097064

FEI Number

3007097064

Entity Name

STERICYCLE, INC.

City/State/Country

Bannockburn, IL, US

Establishment Address

2355 Waukegan Road, Bannockburn, IL 60015, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

STERICYCLE, INC. (Owner Number: 9012522)

Owner / Operator Contact Address

2355 Waukegan Road, --, Bannockburn, IL 60015, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K950898

PMA Number

N/A

All Registered Proprietary Names

Biobox Traptop (Various Sizes) Stericycle Sharps Management Service Reusable Sharps Container Biobox Funnel Top (Various Sizes)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MMK	Container, Sharps	General Hospital	Class 2	880.5570	2008-03-28
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2008-03-28
MMK	Container, Sharps	General Hospital	Class 2	880.5570	2014-01-06
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2008-03-28
MMK	Container, Sharps	General Hospital	Class 2	880.5570	2008-03-28

Official Correspondent

William Nolton

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

STERICYCLE, INC.

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3012237654	Stericycle, Inc.	Aurora, IL, US

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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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007097064. Last updated year: 2026. Please use registration number 3007097064 when referencing this establishment in official correspondence.