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Complete Monocular wireless Smart Cam system with Goggles Flex

FDA UDI

Class II (US FDA UDI)

by Synapsys, Inc.

Identity

Trade Name
Complete Monocular wireless Smart Cam system with Goggles Flex FDA UDI
Generic Name
Electronystagmograph FDA UDI
Device Name
Complete Monocular wireless Smart Cam system with Goggles Flex FDA UDI
Model / Reference
SY.VNS.WIFI FDA UDI
Description
Complete Monocular wireless Smart Cam system with Goggles Flex FDA UDI

Identifiers

Catalog Number
SY.VNS.WIFI FDA UDI
Primary DI / UDI-DI
03760184931527 FDA UDI
510(k) Number
K163558 FDA UDI
FDA Product Code
GWN FDA UDI
GMDN Term
Electronystagmograph FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1460 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electronystagmograph

Complete Monocular wireless Smart Cam system with Goggles Flex by Synapsys, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electronystagmograph.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Synapsys, Inc.

Sources (1)

  • FDA UDI 0e203d69-e9d8-461b-b4d6-c39ca5b1a184 35 fields · synced Jun 8, 2026