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Cerabien™

FDA UDI

Class II (US FDA UDI)

by Kuraray Noritake Dental Inc.

Identity

Trade Name
CERABIEN™ FDA UDI
Generic Name
Dental appliance fabrication material, ceramic FDA UDI
Device Name
SBNW0 200g FDA UDI
Model / Reference
103-0333KA FDA UDI
Description
SBNW0 200g FDA UDI

Identifiers

Primary DI / UDI-DI
EKUR1030333KA0 FDA UDI
510(k) Number
K992023 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

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental appliance fabrication material, ceramic

Cerabien™ by Kuraray Noritake Dental Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Sources (1)

  • FDA UDI d233a45b-b3a1-4958-8e6e-660b02675591 34 fields · synced Jun 6, 2026