Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3002649826

FEI Number

3002649826

Entity Name

ELITE MANUFACTURING

City/State/Country

Jarvis Ontario, CA

Establishment Address

692 nanticoke creek pkwy, Jarvis Ontario N0a 1j0, CA

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

ELITE MANUFACTURING (Owner Number: 9050013)

Owner / Operator Contact Address

692 nanticoke creek pkwy, Jarvis, CA-ON N0a 1j0, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ELITE ELITE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
INQ	Table, Powered	Physical Medicine	Class 1	890.3760	2002-03-04
INW	Table, Mechanical	Physical Medicine	Class 1	890.3750	2002-03-04

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

ELITE MANUFACTURING

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 3002649826. Last updated year: 2026. Please use registration number 3002649826 when referencing this establishment in official correspondence.