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Luminant

FDA UDI

Class I (US FDA UDI)

by Fourstar Group Inc.

Identity

Trade Name
LUMINANT FDA UDI
Generic Name
Oral care kit, reusable FDA UDI
Device Name
LUMINANT ORAL CARE KIT 4PC FDA UDI
Model / Reference
64409357A FDA UDI
Description
LUMINANT ORAL CARE KIT 4PC FDA UDI

Identifiers

Primary DI / UDI-DI
00049696509688 FDA UDI
FDA Product Code
EFW FDA UDI
GMDN Term
Oral care kit, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6855 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Oral care kit, reusable

Luminant by Fourstar Group Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Oral care kit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fourstar Group Inc.

Sources (1)

  • FDA UDI 9f0cee19-bc44-4215-825f-2554e13855f8 33 fields · synced May 30, 2026