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ALMA VEIL +1 more model

FDA UDI

Class II (US FDA UDI)

by Wontech Co., Ltd

Identity

Trade Name
ALMA VEIL; V-Laser FDA UDI
Generic Name
General/multiple surgical solid-state laser system FDA UDI
Device Name
Long pulsed Nd:YAG Laser System FDA UDI
Model / Reference
ALMA VEIL; V-Laser FDA UDI
Description
Long pulsed Nd:YAG Laser System FDA UDI

Identifiers

Primary DI / UDI-DI
08800022304016 FDA UDI
510(k) Number
K231054 FDA UDI
K251094 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
General/multiple surgical solid-state laser system FDA UDI
Models / Variants
ALMA VEIL FDA UDI
V-Laser 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General/multiple surgical solid-state laser system

ALMA VEIL +1 more model by Wontech Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — 2 models — regulatory data on deviCERTS

Similar devices

Also classified as General/multiple surgical solid-state laser system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wontech Co., Ltd

Sources (1)

  • FDA UDI 65e1981e-2e24-4679-ae97-787606bc5b59 34 fields · synced May 31, 2026