Stericycle, Inc.

FDA Device Registration & Listing · Aurora, IL, US · Registration 3012237654

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3012237654
FEI Number
3012237654
Entity Name
Stericycle, Inc.
City/State/Country
Aurora, IL, US
Establishment Address
3557 Butterfield Rd Ste 151, Aurora, IL 60502, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
STERICYCLE, INC. (Owner Number: 9012522)
Owner / Operator Contact Address
2355 Waukegan Road, --, Bannockburn, IL 60015, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K063722
PMA Number
N/A

All Registered Proprietary Names

Sekurit Sharps Collection 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 2015-12-17

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
3007097064 STERICYCLE, INC. Bannockburn, IL, US

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3007097064 STERICYCLE, INC. Bannockburn, IL, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012237654. Last updated year: 2026. Please use registration number 3012237654 when referencing this establishment in official correspondence.
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