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illuvinate Starter Kit

FDA UDI

Class II (US FDA UDI)

by Luma Therapeutics

Identity

Trade Name
illuvinate Starter Kit FDA UDI
Generic Name
Light-energy skin surface treatment system applicator FDA UDI
Device Name
Ultraviolet Light system FDA UDI
Model / Reference
CAT0582 FDA UDI
Description
Ultraviolet Light system FDA UDI

Identifiers

Primary DI / UDI-DI
10860228002104 FDA UDI
510(k) Number
K173436 FDA UDI
FDA Product Code
FTC FDA UDI
GMDN Term
Light-energy skin surface treatment system applicator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4630 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Light-energy skin surface treatment system applicator

illuvinate Starter Kit by Luma Therapeutics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Light-energy skin surface treatment system applicator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Luma Therapeutics

Sources (1)

  • FDA UDI 7e9129c7-e94b-48cb-8c13-c9b899648b60 34 fields · synced May 30, 2026