Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010508078

FEI Number

3010508078

Entity Name

Keter Canada Inc.

City/State/Country

Milton Ontario, CA

Establishment Address

205 Market Drive, Milton Ontario L9T 4Z7, CA

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Keter Canada, Inc. (Owner Number: 10045078)

Owner / Operator Contact Address

205 Market Drive, Milton, CA-ON L9T 4Z7, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K071517

PMA Number

N/A

All Registered Proprietary Names

AP Medical Community Container PBS 12 Lt AP 60 DUO (18 Gal DUO lid) AP 50 DUO (12 Gal DUO lid) AP Medical AP 30 DUO (8 Gal DUO lid) AP 60 MONO (18 Gal MONO lid) AP 30 MONO (8 Gal MONO lid) AP 50 MONO (12 Gal MONO lid) AP 5.4 QT

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MMK	Container, Sharps	General Hospital	Class 2	880.5570	2026-05-27
MMK	Container, Sharps	General Hospital	Class 2	880.5570	2014-06-04

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Keter Canada, 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 3010508078. Last updated year: 2026. Please use registration number 3010508078 when referencing this establishment in official correspondence.