← Back to catalogue

Voguenow

FDA UDI

Class II (US FDA UDI)

by Guangdong Newdermo Biotech Co., Ltd.

Identity

Trade Name
VOGUENOW FDA UDI
Generic Name
Blue/red/infrared phototherapy lamp FDA UDI
Device Name
VOGUENOW LUMINX LED LIGHT THERAPY MASK FDA UDI
Model / Reference
FM-02 FDA UDI
Description
VOGUENOW LUMINX LED LIGHT THERAPY MASK FDA UDI

Identifiers

Primary DI / UDI-DI
06974020960986 FDA UDI
510(k) Number
K223544 FDA UDI
FDA Product Code
OHS FDA UDI
OLP FDA UDI
ILP FDA UDI
GMDN Term
Blue/red/infrared phototherapy lamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 FDA UDI
890.3700 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

Yes

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blue/red/infrared phototherapy lamp

Voguenow by Guangdong Newdermo Biotech Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blue/red/infrared phototherapy lamp.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 91c53a3e-da95-4d7a-8002-9fcb94e0a483 35 fields · synced Jun 1, 2026