Canon Inc.

4 catalogue numbers from CR-2 AF, listed by Canon Inc., Japan, under Camera, Ophthalmic, Ac-Powered. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
4catalogue numbers in this listing
7510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (1), Shanghai (1), Chongqing (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code HKI
Manufacturer City Province Registered as Device types
Shanghai Mediworks Precision Instruments Co., Ltd. Shanghai Shanghai Contract manufacturer 13
Taizhou City K&W International Trade Co., Ltd. Jiangyan Jiangsu Repacker / relabeller 38
Chongqing BIO Newvision Medical Equipment Ltd. Chongqing Chongqing Manufacturer 2

Record

Regulatory record for Canon Inc.
Listed by Canon Inc., Japan
FDA product code HKI
Device type Camera, Ophthalmic, Ac-Powered
Device class Class 2
Regulation 21 CFR 886.1120
Establishment Contract manufacturer, Specification developer, Manufacturer
510(k) K092565
Record published 2016-09-24
Record revised 2026-03-20 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries serial number

Catalogue Numbers

Catalogue numbers for Canon Inc.
Catalogue number Size Status
CR-2 AF In distribution
CX-1 In distribution
CR-2 Plus AF In distribution
CR-10 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Jedmed Jedmed Instrument Company 15
Neolight Neolight, LLC 11
Natus Xltek 6
RetCam Envision Natus Medical Denmark ApS 6
3nethra Forus Health Pvt.ltd., 6
iCam Optovue, Inc. 5
iFusion Optovue, Inc. 5
Camera, Ophthalmic, Ac-Powered Chongqing Kanghuaruiming S&T Co., Ltd.. 4
3D Optical Coherence Tomography 3D OCT-1(Type:Maestro2) Topcon Corp. 3
Retinal Camera TRC-50DX Topcon Corp. 3
NON-Mydriatic Retinal Camera TRC-NW400 Topcon Corp. 2
Visionix Luneau Technology Operations 2

Showing 12 of 123. All products under Camera, Ophthalmic, Ac-Powered

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K241049 2024-05-15
K201122 2020-07-23
K111612 2011-09-14
K090466 2009-03-23
K080883 2008-04-24
K063717 2007-01-23
K041546 2004-06-23

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer