Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2022883

FEI Number

2022883

Entity Name

CONVAID PRODUCTS LLC

City/State/Country

TORRANCE, CA, US

Establishment Address

2830 California St, TORRANCE, CA 90503, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Convaid Products, LLC (Owner Number: 10056491)

Owner / Operator Contact Address

2830 California Street, Torrance, CA 90503, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K032402

PMA Number

N/A

All Registered Proprietary Names

Flyer Transit Flyer Trekker Trekker Transit Safari Special Tomato Metro Scout Cruiser EZRider Convertible Vivo Rodeo Reno

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LBE	Stroller, Adaptive	Physical Medicine	Class 1	890.3850	2017-12-14
IOR	Wheelchair, Mechanical	Physical Medicine	Class 1	890.3850	2017-12-14
IOR	Wheelchair, Mechanical	Physical Medicine	Class 1	890.3850	2017-12-14
LBE	Stroller, Adaptive	Physical Medicine	Class 1	890.3850	2017-12-14
LBE	Stroller, Adaptive	Physical Medicine	Class 1	890.3850	2017-12-14
KNO	Accessories, Wheelchair	Physical Medicine	Class 1	890.3910	2025-11-20
INM	Chair, With Casters	Physical Medicine	Class 1	890.3100	2017-12-14
IOR	Wheelchair, Mechanical	Physical Medicine	Class 1	890.3850	2017-12-14

Official Correspondent

Giovanny Espinosa

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Convaid Products, LLC

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
K935211	Brookefield Hunter, Inc.	WALK N CHAIR	1994-02-02
K832685	Health America	WHEELCHAIR-VARIOUS MODELS	1983-09-20

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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2022883. Last updated year: 2026. Please use registration number 2022883 when referencing this establishment in official correspondence.