Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003751839

FEI Number

3003751839

Entity Name

Equipro Equipements D'Esthetique Inc.

City/State/Country

Montreal Quebec, CA

Establishment Address

11970 Boulevard Albert-Hudon, Montreal Quebec H1G 3K3, CA

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Equipro Beauty USA, Inc. (Owner Number: 10027402)

Owner / Operator Contact Address

2425 Main Street, Isle La Motte, VT 05463, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Equipro Equipements D'Esthetique Inc. Equipro Equipements D'Esthetique Inc. Equipro Equipements D'Esthetique Inc. Equipro Equipements D'Esthetique Inc. Equipro Equipements D'Esthetique Inc.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KFZ	Humidifier, Non-Direct Patient Interface (Home-Use)	Anesthesiology	Class 1	868.5460	2017-11-21
INM	Chair, With Casters	Physical Medicine	Class 1	890.3100	2017-11-21
FNK	Bed, Hydraulic, Adjustable Hospital	General Hospital	Class 1	880.5110	2008-11-17
IRT	Pad, Heating, Powered	Physical Medicine	Class 2	890.5740	2011-05-05
LLI	Bed, Therapeutic, Ac-Powered, Adjustable Home-Use	General Hospital	Class 2	880.5100	2017-11-21

Official Correspondent

No official correspondent registered.

US Agent Details

STEPHANE FANTIN Email: LAURENT@EQUIPRO-BTY.COM Phone: (518) 3104940

Related Public Records

Same Entity

Equipro Beauty USA, 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
K881862	Thermo Body Wrap Systems, Inc.	THERMO-BODY-WRAP SYSTEM	1988-10-13

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0011-2015	Nemschoff Chairs, Inc. 909 N 8th St 2218 Julson Ct Sheboygan WI 53081-4056	1	Nemschooff, Model Numbers - Serenity II:790-12, Serenity III: 791-12, Serenity III Exam: 791-12E, and Serenity IIS: 792-12. Designed to provide patient comfort during patient treatment sessions. The chair may include a manual control reclining mechanism. Customer configurable models are also available. The Serenity III Exam 791-12E was discontinued 11/1/2010.
Z-0031-2013	Winco Mfg., LLC	1	Caremor Cliner"*Manufactured By WincoOcala, FL 34474 www.wincomfg.comModel No. 536 Serial No. 536A-101475" Literature: "Caremor Cliner 5351/5361WincoISO 9001-2008 CertifiedOur most comfortable and versatile reclinerEase of operation, outstanding durability, and exceptional value have made this one of our bestselling recliners. The Caremor Cliner provides patient comfort and support as well as user friendly features.KEY FEATURE'SInfinite positioning backPadded armrests w/arm guardWebbed elastic suspension back and seatRemovable side panelsContinuous seat & legrest cushion5351 w/tray5361 w/out tray1.800.237.33775516 SW 1st LaneOcala, Florida 34474www.wincomfg.comProudly Made in the USA*" Patient recliner chair
Z-0032-2013	Winco Mfg., LLC	1	Caremor Cliner is labeled in part: "*Manufactured By WincoOcala, FL 34474 www.wincomfg.comModel No. 535 Serial No. 535A-104522" Literature: "Caremor Cliner 5351/5361WincoISO 9001-2008 CertifiedOur most comfortable and versatile reclinerEase of operation, outstanding durability, and exceptional value have made this one of our bestselling recliners. The Caremor Cliner provides patient comfort and support as well as user friendly features.KEY FEATURE'SInfinite positioning backPadded armrests w/arm guardWebbed elastic suspension back and seatRemovable side panelsContinuous seat & legrest cushion5351 w/tray5361 w/out tray1.800.237.33775516 SW 1st LaneOcala, Florida 34474www.wincomfg.comProudly Made in the USA*" Patient recliner chair

Similar Registrations

Registration Number	Establishment Name	Location
3014153468	JIANGMEN HONETIAN TECHNOLOGY CO., LTD	Jiangmen Guangdong, CN
1000190272	LASKO PRODUCTS LLC	West Chester, PA, US
3022528821	J SUMMIT CO., LTD.	Chomthong Krung Thep Maha Nakhon, TH
3011919098	NINGBO JUST SOON INDUSTRIAL LIMITED	Ningbo Zhejiang, CN
3004264602	SHANGHAI FOREIGN TRADE ENTERPRISES PUDONG CO., LTD.	Shanghai, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003751839. Last updated year: 2026. Please use registration number 3003751839 when referencing this establishment in official correspondence.