Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011197286

FEI Number

3011197286

Entity Name

Jintronix Inc.

City/State/Country

Montreal Quebec, CA

Establishment Address

5455 De Gaspe Ave, Suite 710, Montreal Quebec H2T 3B3, CA

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Ludica Health Inc. (Owner Number: 10047062)

Owner / Operator Contact Address

999 3rd Ave., Suite 3400, Seattle, WA 98104, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K143034

PMA Number

N/A

All Registered Proprietary Names

LudoFit PRO Jintronix Jintronix 2 LudoFit Home

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LXJ	Interactive Rehabilitation Exercise Devices	Physical Medicine	Class 2	890.5360	2016-11-02

Official Correspondent

Mark Evin

US Agent Details

Mark Evin Email: mark@jintronix.com Phone: (888) 6236462

Related Public Records

Same Entity

Ludica Health Inc.

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

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3013517146	NeuroXtherapeutics SA	Lausanne Vaud, CH
3015786441	QUALISYS AB	Goteborg Vastra Gotaland, SE
1000377231	VICON MOTION SYSTEMS INC	CENTENNIAL, CO, US
8021839	VICON MOTION SYSTEMS, LTD.	YARNTON Oxfordshire, GB
3005998761	BTS SPA	VIGONZA Padova, IT

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011197286. Last updated year: 2026. Please use registration number 3011197286 when referencing this establishment in official correspondence.