Kinetic Wi-Fi Wireless VNG Ulmer System With Goggles Flex

Catalogue number SY.VNG.WIFI_CINE, listed by Synapsys SA, France, under Nystagmograph. 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
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (2), Beijing (1).

Chinese manufacturers registered for FDA product code GWN
Manufacturer City Province Registered as Device types
Isen Tech.&Trading Co., Ltd. Beijing Beijing Manufacturer 2
E-Business International Inc. Shenzhen Guangdong Exporter 2
Huizhou Maxway Technology Co., Ltd. Huizhou Guangdong Contract manufacturer 2

Record

Regulatory record for Kinetic Wi-Fi wireless VNG Ulmer system with Goggles Flex
Listed by Synapsys SA, France
FDA product code GWN
Device type Nystagmograph
Device class Class 2
Regulation 21 CFR 882.1460
510(k) K163558
Record published 2017-06-27
Record revised 2018-07-06 (version 3)

Specifications

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

Catalogue Numbers

Catalogue numbers for Kinetic Wi-Fi wireless VNG Ulmer system with Goggles Flex
Catalogue number Size Status
SY.VNG.WIFI_CINE In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
GN Otometrics A/S Natus Medical Denmark ApS 17
Interacoustics Interacoustics A/S 15
VNG Inventis SRL 9
Instrumentation Difra SA Instrumentation Difra SA 8
Nystagmograph Medtronic PS Medical 7
Instrumentation Difra Instrumentation Difra SA 7
Otometrics Natus Medical Denmark ApS 5
Vestibular First Vestibular First 4
Micromedical Technologies Micromedical Technologies, Inc. 3
Complete Monocular wireless Smart Cam system with Xpress mask Synapsys SA 2
Synapsys Vhit Inventis SRL 2
EYE-Sync Neurosync, Inc. 2

Showing 12 of 37. All products under Nystagmograph

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K163558 2017-03-23
K982103 1998-09-11

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