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New Hue® VF Porcelain Anteriors

FDA UDI

Class II (US FDA UDI)

by Dentsply International

Identity

Trade Name
New Hue® VF Porcelain Anteriors FDA UDI
Generic Name
Ceramic artificial teeth FDA UDI
Model / Reference
B66 L 3M FDA UDI

Identifiers

Catalog Number
13163 FDA UDI
Primary DI / UDI-DI
D00113163LB663M0 FDA UDI
FDA Product Code
ELL FDA UDI
GMDN Term
Ceramic artificial teeth FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3920 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ceramic artificial teeth

New Hue® VF Porcelain Anteriors by Dentsply International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ceramic artificial teeth.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dentsply International

Sources (1)

  • FDA UDI e86ef8f4-53f2-4f92-99ee-2b55c99e89b2 34 fields · synced Jun 1, 2026