Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016076693

FEI Number

3016076693

Entity Name

KUBE INNOVATION INC.

City/State/Country

Montreal Quebec, CA

Establishment Address

315-5524 Saint-Patrick Street, Montreal Quebec H4E1A8, CA

Establishment Type(s)

Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Kube Innovation Inc. (Owner Number: 10082048)

Owner / Operator Contact Address

315-5524 Saint-Patrick Street, Montreal, CA-QC H4E1A8, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Innobyte Clinical Package

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LBB	Dynamometer, Ac-Powered	Orthopedic	Class 2	888.1240	2021-07-06

Official Correspondent

Frederik Marcil

US Agent Details

Marc Duey Business: ProMetrics inc Email: regulatory@kubeinnovation.com Phone: (610) 6330403

Related Public Records

Same Entity

Kube Innovation 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 3016076693. Last updated year: 2026. Please use registration number 3016076693 when referencing this establishment in official correspondence.