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TruExpression® Plastic Anteriors

FDA UDI

Class II (US FDA UDI)

by Dentsply International

Identity

Trade Name
TruExpression® Plastic Anteriors FDA UDI
Generic Name
Resin artificial teeth FDA UDI
Model / Reference
B03 U 14G FDA UDI

Identifiers

Catalog Number
16026 FDA UDI
Primary DI / UDI-DI
D00116026UB0314G0 FDA UDI
FDA Product Code
ELM FDA UDI
GMDN Term
Resin artificial teeth FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3590 FDA UDI
Commercial Distribution
Not 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

No

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

TruExpression® Plastic Anteriors by Dentsply International — 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 01d1dd36-e2cf-4ad7-aee0-9da8398c9aac 35 fields · synced May 31, 2026