IMAGEnet 6 Ophthalmic Data System

Catalogue number IMAGEnet 6, listed by Topcon Corp., 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
1catalogue number
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 IMAGEnet 6 Ophthalmic Data System
Listed by Topcon Corp., Japan
FDA product code HKI
Device type Camera, Ophthalmic, Ac-Powered
Device class Class 2
Regulation 21 CFR 886.1120
Establishment Specification developer, Manufacturer, Exporter
Record published 2018-02-07
Record revised 2023-07-31 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number, serial number

Catalogue Numbers

Catalogue numbers for IMAGEnet 6 Ophthalmic Data System
Catalogue number Size Status
IMAGEnet 6 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
Canon Inc. Canon Inc. 4
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

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
K221111 2022-08-29
K141325 2014-10-23
K141481 2014-09-17
K130289 2013-05-10
K100207 2010-02-12
K090115 2009-06-30
K041367 2004-11-05

Recalls Naming This Product

1 recall names this product by its own identifier, the UDI on its label.

Recalls naming the identifiers of IMAGEnet 6 Ophthalmic Data System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Topcon Corp. UDI-DI 2024-09-17 Class II Software design The overlay of visual field test locations on a probability map, as presented in IMAGEnet 6 in the so-called “Hood
Report”, is not appropriate as it can imply a structure/function correlation for which clinical evidence is not provided
3144 units

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