Lucina Control Wand

FDA UDI

Class I (US FDA UDI)

by Skytron, LLC

Identity

Trade Name: Lucina Control Wand FDA UDI
Generic Name: Fixed examination/treatment room light FDA UDI
Device Name: Control Wand for Lucina 4 FDA UDI
Model / Reference: B5-014-39 FDA UDI
Description: Control Wand for Lucina 4 FDA UDI

Identifiers

Primary DI / UDI-DI: 10841736112080 FDA UDI
FDA Product Code: KZF FDA UDI
GMDN Term: Fixed examination/treatment room light FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.6320 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Fixed examination/treatment room light

Lucina Control Wand by Skytron, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Skytron, LLC

Sources (1)

FDA UDI 130e722c-a0d9-4d8e-997b-cd1ea80345f3 35 fields · synced May 30, 2026