Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012983142

FEI Number

3012983142

Entity Name

CANON VIRGINIA, INC. MEDICAL PRODUCTS GROUP (CVIMPG)

City/State/Country

Newport News, VA, US

Establishment Address

12000 Canon Blvd, Newport News, VA 23606, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Canon Virginia, Inc. Medical Products Group (CVIMPG) (Owner Number: 10059097)

Owner / Operator Contact Address

12000 Canon Blvd., Newport News, VA 23606, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

AiroCide COVID 19

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FRA	Purifier, Air, Ultraviolet, Medical	General Hospital	Class 2	880.6500	2023-05-22
QKP	Coronavirus Antigen Detection Test System.	Unknown	Class N	N/A	2023-09-12

Official Correspondent

James Mershon

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Canon Virginia, Inc. Medical Products Group (CVIMPG)

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0001-2023	Jiangsu Well Biotech Co., Ltd. No	N	Jiangsu Well Biotech Co.,Ltd. AND SDI LABS COVID-19 Ag Rapid Test Device - Cat#: CO-02

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012983142. Last updated year: 2026. Please use registration number 3012983142 when referencing this establishment in official correspondence.