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Luminant

FDA UDI

Class I (US FDA UDI)

by Fourstar Group Inc.

Identity

Trade Name
LUMINANT FDA UDI
Generic Name
Ionic electric toothbrush FDA UDI
Device Name
LUMINANT BO TB W/REMOVEABLE HD FDA UDI
Model / Reference
11012436DA FDA UDI
Description
LUMINANT BO TB W/REMOVEABLE HD FDA UDI

Identifiers

Primary DI / UDI-DI
00049696736701 FDA UDI
FDA Product Code
JEQ FDA UDI
GMDN Term
Ionic electric toothbrush FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6865 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

Yes

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: Ionic electric toothbrush

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

Similar devices

Also classified as Ionic electric toothbrush.

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 f1ef23e0-53ff-442e-9547-7dcd1c8e8f44 33 fields · synced May 30, 2026