Lipiview Ocular Surface Interferometer

Assembly Pkgd Lipiview 1 - Intl

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
4510(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 Lipiview Ocular Surface Interferometer
Listed by TearScience, Inc., United States
FDA product code HKI
Device type Camera, Ophthalmic, Ac-Powered
Device class Class 2
Regulation 21 CFR 886.1120
Establishment Specification developer, Manufacturer
Record published 2016-09-23
Record revised 2019-10-04 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number
Storage Handling environment temperature 5 to 60 °C

Catalogue Numbers

Catalogue numbers for Lipiview Ocular Surface Interferometer
Catalogue number Size Status
LVI-1001 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
K182506 2018-12-10
K152869 2016-01-14
K122481 2012-12-31
K091935 2009-10-23

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