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Hair Removal Laser

FDA UDI

Class II (US FDA UDI)

by Tria Laser Inc

Identity

Trade Name
HAIR REMOVAL LASER FDA UDI
Generic Name
Dermatological diode laser system FDA UDI
Device Name
Hair Removal Laser 4X, White with Fuchsia FDA UDI
Model / Reference
HRL 4X FDA UDI
Description
Hair Removal Laser 4X, White with Fuchsia FDA UDI

Identifiers

Catalog Number
3724 FDA UDI
Primary DI / UDI-DI
B5863724 FDA UDI
510(k) Number
K090820 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
Dermatological diode laser 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dermatological diode laser system

Hair Removal Laser by Tria Laser Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dermatological diode laser system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tria Laser Inc

Sources (1)

  • FDA UDI 2116cb16-0526-48ed-a194-0b5f7d0faa6c 36 fields · synced May 31, 2026