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n!ce Zirconia

FDA UDI

Class II (US FDA UDI)

by Institut Straumann SA

Identity

Trade Name
n!ce Zirconia FDA UDI
Generic Name
Dental appliance fabrication material, ceramic FDA UDI
Device Name
n!ce® ZirconiaHT, Mono B3, 14mm FDA UDI
Model / Reference
Milling Materials FDA UDI
Description
n!ce® ZirconiaHT, Mono B3, 14mm FDA UDI

Identifiers

Catalog Number
010.7222US FDA UDI
Primary DI / UDI-DI
07630031767493 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
Not 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

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Height — 14 Millimeter FDA UDI

n!ce Zirconia by Institut Straumann SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 22714106-a557-4833-88f1-fb942aca6148 37 fields · synced May 31, 2026