AMYLIOR, INC.

FDA Device Registration & Listing · Vaudreuil-Dorion Quebec, CA · Registration 9615410

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
9615410
FEI Number
3003767999
Entity Name
AMYLIOR, INC.
City/State/Country
Vaudreuil-Dorion Quebec, CA
Establishment Address
3190 F.X. Tessier, Vaudreuil-Dorion Quebec J7V 5V5, CA
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
AMYLIOR, INC. (Owner Number: 9036363)
Owner / Operator Contact Address
3190 F.X. Tessier, Vaudreuil-Dorion, CA-QC J7V 5V5, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K011006
PMA Number
N/A

All Registered Proprietary Names

Interface Tilt PTS 50 CG PTS 50 Alltrack Continent Globe, Stella, CGR CGair Amyseat tilt/recline seating Amyseat Amyseat II tilt/recline seating Amyseat II

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ITI Wheelchair, Powered Physical Medicine Class 2 890.3860 2008-01-28
ITI Wheelchair, Powered Physical Medicine Class 2 890.3860 2009-12-30
ITJ Walker, Mechanical Physical Medicine Class 1 890.3825 2018-01-08
KIC Cushion, Flotation Physical Medicine Class 1 890.3175 2017-04-10
ITI Wheelchair, Powered Physical Medicine Class 2 890.3860 2008-01-28

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

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K853594 Vessa , Ltd. VESSA FLIVVA 1985-09-24
K142783 Heartway Medical Products Co., Ltd. HEARTWAY Electrically Powered Wheelchair P27 2015-06-12

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0005-2018 Permobil, Ab Arvaltsvagen 10 2
Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II f) C500 CORPUS II LR
Z-0006-2018 Permobil, Ab Arvaltsvagen 10 2
Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500
Z-0039-2007 Eagle Parts and Products 2
Eagle Parts and Products Model 624EZ Power Wheel Chairs with internally threaded wheel mount motors.
Z-0040-2007 Eagle Parts and Products 2
Eagle Parts and Products Model 624Mini Power Wheel Chairs with internally threaded wheel mount motors.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9615410. Last updated year: 2026. Please use registration number 9615410 when referencing this establishment in official correspondence.
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