← Back to catalogue

KATANA™ Zirconia ONE

FDA UDI

Class II (US FDA UDI)

by Kuraray Noritake Dental Inc.

Identity

Trade Name
KATANA™ Zirconia ONE FDA UDI
Generic Name
Dental appliance fabrication material, ceramic FDA UDI
Device Name
For IMPLANT S A3.5 FDA UDI
Model / Reference
125-9683KA FDA UDI
Description
For IMPLANT S A3.5 FDA UDI

Identifiers

Primary DI / UDI-DI
EKUR1259683KA0 FDA UDI
510(k) Number
K233285 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Dental appliance fabrication material, ceramic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3630 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
MRI Safety
MR Conditional FDA UDI

Category: Dental appliance fabrication material, ceramic

KATANA™ Zirconia ONE 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 6d912804-0f35-4be6-b8d3-288b0d31fb42 35 fields · synced Jun 1, 2026