Broda LP

FDA Device Registration & Listing · Kitchener Ontario, CA · Registration 8043392

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
8043392
FEI Number
3007074101
Entity Name
Broda LP
City/State/Country
Kitchener Ontario, CA
Establishment Address
560 Bingemans Centre Dr, Kitchener Ontario N2B3X9, CA
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Broda LP (Owner Number: 9001296)
Owner / Operator Contact Address
560 Bingemans Centre Drive, --, Kitchener, CA-ON N2B3X9, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

(Broda LP) (Broda LP) (Broda LP) (Broda LP) (Broda LP) (Broda LP) Traversa Transport Wheelchair (Broda LP)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IMM Footrest, Wheelchair Physical Medicine Class 1 890.3920 2016-05-18
KMN Chair And Table, Medical General Hospital Class 1 880.6140 2003-10-03
IMX Board, Lap, Wheelchair Physical Medicine Class 1 890.3910 2010-01-21
INN Chair, Adjustable, Mechanical Physical Medicine Class 1 890.3100 2000-05-11
KNO Accessories, Wheelchair Physical Medicine Class 1 890.3910 2009-06-26
IMS Support, Head And Trunk, Wheelchair Physical Medicine Class 1 890.3910 2010-01-21
IOR Wheelchair, Mechanical Physical Medicine Class 1 890.3850 2008-03-27
IMQ Attachment, Narrowing, Wheelchair Physical Medicine Class 1 890.3920 2016-05-18

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

Broda LP
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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8043392. Last updated year: 2026. Please use registration number 8043392 when referencing this establishment in official correspondence.
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