Istand

iStand 2

Registry build 21.09.26
7manufacturers in China registered for this device type
1catalogue number
7510(k) clearances naming this product code
4recalls on this code

Who Else Makes It

Concentrated in Jiangsu (5), Beijing (1), Jiangxi (1).

Chinese manufacturers registered for FDA product code HLI
Manufacturer City Province Registered as Device types
Beijing Hongdee Corporation Beijing Beijing Private-label distributor 43
Lianyungang Tiannuo Optical Instrument Co., Ltd. Lianyungang Jiangsu Contract manufacturer 31
Shanghai Link Instruments Co., Ltd. Changzhou Jiangsu Manufacturer 21
Zumax Medical Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Suzhou Raish Meditech Co., Ltd. Suzhou Jiangsu Manufacturer 4
Jiang XI BIG Vision Medical Technology Co., Ltd. Ganzhou Jiangxi Manufacturer 3
Robotrak Technologies Co., Ltd. Nanjing Jiangsu Manufacturer 1

Record

Regulatory record for iStand
Listed by Optovue, Inc., United States
FDA product code HLI
Device type Ophthalmoscope, Ac-Powered
Device class Class 2
Regulation 21 CFR 886.1570
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K103266
Record published 2016-08-03
Record revised 2021-08-09 (version 4)

Specifications

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

Catalogue Numbers

Catalogue numbers for iStand
Catalogue number Size Status
iStand In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Welch Allyn, Inc. Welch Allyn, Inc. 90
Amico Diagnostic Station Amico Diagnostic Incorporated 55
iVue Optovue, Inc. 27
Amico Diagnostic Wallboard Amico Diagnostic Incorporated 19
Amico Diagnostic Rollstand Amico Diagnostic Incorporated 14
iScan Optovue, Inc. 7
zumax Zumax Medical Co., Ltd. 6
Jedmed Jedmed Instrument Company 3
RTVue XR Avanti Optovue, Inc. 3
Amico Diagnostic Ophthalmoscope Amico Diagnostic Incorporated 3
Laser Speckle Flowgraphy Lsfg-Navi Softcare Co., Ltd. 2
Panoramic Ophthalmoscope Optos Public Limited Company 1

Showing 12 of 46. All products under Ophthalmoscope, Ac-Powered

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K153080 2016-02-11
K133892 2014-03-19
K121739 2013-01-18
K120238 2012-04-03
K103266 2011-06-03
K101505 2010-09-15
K100861 2010-06-17

Recalls

3 of these are Class II. Class II means a temporary or reversible health consequence. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. 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
2017-07-27 Class II Other FDA determined that a 510(k) is needed for the Vault Mapping software (also known as Lens Fitting). 326 devices 2021-04-12
2017-07-27 Class II Other FDA determined that a 510(k) is needed for the Vault Mapping software (also known as Lens Fitting). 326 devices 2021-04-12
2016-03-16 Class II Under Investigation by firm A software anomaly was detected that affects Optovue iVue and iVue 500 with Normative Database that may display images of the same eye rather than right and left if user scrolls on the map. 40 2017-04-04
2013-05-14 Class III Software design Colors from the NDB comparison for Ganglion Cell Complex thickness in the singular OU report in iVue version 3.0 (US) and 3.1(international) are different from those in the individual iWellness ID and OS reports. ~329 users 2013-10-24

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