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Iluzion

FDA UDI

Class II (US FDA UDI)

by Opa Dental, Llc

Identity

Trade Name
Iluzion FDA UDI
Generic Name
Dental appliance fabrication material, ceramic FDA UDI
Device Name
Iluzion dental zirconia FDA UDI
Model / Reference
LZN9810D3 FDA UDI
Description
Iluzion dental zirconia FDA UDI

Identifiers

Catalog Number
LZN9810D3 FDA UDI
Primary DI / UDI-DI
D815LZN9810D30 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

Iluzion by Opa Dental, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, ceramic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Opa Dental, Llc

Sources (1)

  • FDA UDI b78222d4-2f6f-4af4-a378-c9d1ee2ca0a0 34 fields · synced May 31, 2026