Arjo Canada Inc.

FDA Device Registration & Listing · Mississauga Ontario, CA · Registration 3010010434

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
3010010434
FEI Number
3010010434
Entity Name
Arjo Canada Inc.
City/State/Country
Mississauga Ontario, CA
Establishment Address
550 Matheson Blvd. East, Unit 7, Mississauga Ontario L4Z 4G3, CA
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
ArjoHuntleigh AB (Owner Number: 10036598)
Owner / Operator Contact Address
Hans Michelsensgatan 10, Malmo, SE-M 211 20, SE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

HARMONIE (FOREIGN EXPORTER) SYSTEM 2000 (FOREIGN EXPORTER) SARA PLUS (FOREIGN EXPORTER ONLY) Various Arjo slings Arjo Disposable Slide sheets; Arjo Disposable Slide Tube

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ILJ Bath, Hydro-Massage Physical Medicine Class 2 890.5100 2020-06-10
FSA Lift, Patient, Non-Ac-Powered General Hospital Class 1 880.5510 2011-05-17
IKX Aid, Transfer Physical Medicine Class 1 890.5050 2020-06-05

Official Correspondent

No official correspondent registered.

US Agent Details

Darren Demerritt Business: Arjo Inc Email: darren.demerritt@arjo.com Phone: (425) 3089587

Related Public Records

Same Entity

ArjoHuntleigh AB
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3012292104 Arjo Dominican Republic Itabo, Haina San Cristobal, DO
3007518069 ARJOHUNTLEIGH LOGISTICS Eindhoven Noord-Brabant, NL

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0013-2018 Handicare Usa Inc 1
PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered
Z-0014-2018 Handicare AB Maskinvagen 1
Carina Mobile Lifts, Models: a) Carina350EM, REF 6060011 b) Carina350EML, REF 60600012 c) Carina350EE, REF 60600009

Similar Registrations

Registration Number Establishment Name Location
3007420694 ArjoHuntleigh Polska Sp. zo.o. Poznan Wielkopolskie, PL
3042227943 MULTI GARMEN INDONESIA BOGOR Jawa Barat, ID
3016446653 Shenzhen Margotan Tech Co., Ltd. shenzhen Guangdong, CN
1922538 Penner Patient Care, INC Aurora, NE, US
3027517735 LIANJIA (ZHONGSHAN) GONGMAO CO.LTD Zhongshan Guangdong, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010010434. Last updated year: 2026. Please use registration number 3010010434 when referencing this establishment in official correspondence.
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