Auto REF/Keratometer

The NIDEK AUTO REF/KERATOMETER ARK-1s measures spherical, cylindrical refractive errors, and cylinder axis from the refractive status of the patient’s eye. In addition, subjective test is…

Registry build 21.09.26

The NIDEK AUTO REF/KERATOMETER ARK-1s measures spherical, cylindrical refractive errors, and cylinder axis from the refractive status of the patient’s eye. In addition, subjective test is performed with the built-in charts and lenses for subjective measurement. The keratometer measures the corneal curvature radius (corneal refractive power), principal meridian directions, and corneal cylindrical power.

17manufacturers in China registered for this device type
3catalogue numbers in this listing
8510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Jiangsu (4), Shanghai (4), Beijing (2). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HKO
Manufacturer City Province Registered as Device types
Wuxi Zontai Int’l Corporation Ltd. Wuxi Jiangsu Contract manufacturer 22
Taiyuan North China Xinyuan Tech. Center (Co., Ltd.) Taiyuan Shaanxi Contract manufacturer 14
Beijing Hongdee Corporation Beijing Beijing Private-label distributor 43
Taizhou City K&W International Trade Co., Ltd. Jiangyan Jiangsu Repacker / relabeller 38
Lianyungang Tiannuo Optical Instrument Co., Ltd. Lianyungang Jiangsu Contract manufacturer 31
Shanghai Link Instruments Co., Ltd. Changzhou Jiangsu Manufacturer 21
Gino Optical (Shanghai) Co., Ltd. Shanghai Shanghai Manufacturer 15
Shanghai Mediworks Precision Instruments Co., Ltd. Shanghai Shanghai Contract manufacturer 13
Chongqing Sunkingdom Medical Instrument Co., Ltd. Chongqing Chongqing Manufacturer 11
Ningbo Ming Sing Optical R&D Co., Ltd. Ningbo Zhejiang Repacker / relabeller 9
Shenzhen Certainn Technology Co., Ltd. Shenzhen Guangdong Manufacturer 7
Chongqing Yeasn Science-Technology Co., Ltd. Chongqing Chongqing Contract manufacturer 5

Showing 12 of 17. All 17 manufacturers in China registered for Refractometer, Ophthalmic

Record

Regulatory record for Auto REF/Keratometer
Listed by Nidek Incorporated, United States
FDA product code HKO
Device type Refractometer, Ophthalmic
Device class Class 1
Regulation 21 CFR 886.1760
Establishment Specification developer, Manufacturer
Premarket notification Exempt
Record published 2018-04-20
Record revised 2020-12-21 (version 4)

Specifications

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

Catalogue Numbers

Catalogue numbers for Auto REF/Keratometer
Catalogue number Size Status
ARK-1s In distribution
ARK-1 In distribution
ARK-1a In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Righton Right MFG. Co., Ltd. 27
Welch Allyn, Inc. Welch Allyn, Inc. 13
Visionix Right MFG. Co., Ltd. 13
Auto REF/Keratometer Ningbo Ming Sing Optical R&D Co., Ltd. 6
Microclear Suzhou Microclear Medical Instruments Co., Ltd. 6
Rexxam Rexxam.co., Ltd. 5
Auto Refractometer Nidek Incorporated 4
plusoptiX 12 Plusoptix Gmbh 4
Auto Refkeratometer Tomey Corporation 4
MediWorks Shanghai Mediworks Precision Instruments Co., Ltd. 3
Auto Refractometer RM-800 Topcon Corp. 3
Yeasn Chongqing Yeasn Science-Technology Co., Ltd. 3

Showing 12 of 52. All products under Refractometer, Ophthalmic

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K902500 1990-07-27
K901513 1990-06-08
K890559 1989-02-27
K882191 1988-07-01
K861065 1986-04-09
K861062 1986-04-04
K861066 1986-04-04
K831083 1983-06-10

Recalls

2 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2017-12-20 Class II Equipment maintenance There is possibly a difference between the measured dioptric value of the subjective measurement mode and the objective measurement mode on ARK-1s. 63 untis 2019-03-18
2015-06-15 Class II Software design Software bug was found where there was no difference in Total and Corneal high-order aberrations, but differences were found in Internal high-order aberrations. 3836 2016-04-25

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