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Luxen 5g

FDA UDI

Class II (US FDA UDI)

by Dentalmax Co., Ltd

Identity

Trade Name
LUXEN 5G FDA UDI
Generic Name
Dental appliance fabrication material, ceramic FDA UDI
Model / Reference
Luxen ML D98 D4 25T FDA UDI

Identifiers

Primary DI / UDI-DI
08809900566805 FDA UDI
510(k) Number
K241151 FDA UDI
FDA Product Code
EIH FDA UDI
GMDN Term
Dental appliance fabrication material, ceramic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.6660 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental appliance fabrication material, ceramic

The LUXEN 5G dental implant system is a revolutionary product that combines the benefits of ceramic materials with advanced CAD/CAM technology. It's designed for manual and computer-aided design/computer-aided manufacturing (CAD/CAM) processes, ensuring high-quality restorations for patients.

Similar devices

Also classified as Dental appliance fabrication material, ceramic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dentalmax Co., Ltd

Sources (1)

  • FDA UDI 6171088f-ff7b-42d7-88d2-da0978ac19cf 33 fields · synced Jul 12, 2026