Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1000214453

FEI Number

1000214453

Entity Name

AMICO MOBILITY SOLUTIONS

City/State/Country

Richmond Hill Ontario, CA

Establishment Address

122 East Beaver Creek Rd, Richmond Hill Ontario L4B 1G6, CA

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

Amico Mobility Solutions (Owner Number: 10054012)

Owner / Operator Contact Address

122 East Beaver Creek Rd, Richmond Hill, CA-ON L4B 1G6, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Two-Part Radiolucent Stretcher (Poweo 300, Poweo 215, Poweo 200) Lift, patient, non-ac-powered POWEO 300 Patient Lift SHADO 160 XS Shower Trolley

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NZD	Stretcher, Patient Restraint	General Hospital	Class 1	880.6900	2025-08-12
FSA	Lift, Patient, Non-Ac-Powered	General Hospital	Class 1	880.5510	2017-02-01

Official Correspondent

No official correspondent registered.

US Agent Details

Jon Ward Business: AJW Technology Consultants, Inc. Email: usagent@ajwtech.com Phone: (813) 6452855

Related Public Records

Same Entity

Amico Mobility Solutions

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

View Entity Profile →

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

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3005822866	INTERTEK INDUSTRIAL CORP	Jacksonville, FL, US
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000214453. Last updated year: 2026. Please use registration number 1000214453 when referencing this establishment in official correspondence.