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V-IPL Filter AC-415

FDA UDI

Class II (US FDA UDI)

by Viora Ltd

Identity

Trade Name
V-IPL Filter AC-415 FDA UDI
Generic Name
Intense pulsed light skin surface treatment system FDA UDI
Device Name
V-IPL Filter AC-415 FDA UDI
Model / Reference
VTL43030-5 FDA UDI
Description
V-IPL Filter AC-415 FDA UDI

Identifiers

Catalog Number
VTL43030-5 FDA UDI
Primary DI / UDI-DI
07290016746112 FDA UDI
510(k) Number
K133837 FDA UDI
K142093 FDA UDI
K152611 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
Intense pulsed light skin surface treatment system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intense pulsed light skin surface treatment system

V-IPL Filter AC-415 by Viora Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intense pulsed light skin surface treatment system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Viora Ltd

Sources (1)

  • FDA UDI 525014d4-2388-4b82-b940-73b07d3529ec 36 fields · synced May 30, 2026