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DENTSPLY TruByte® Characterized Lucitone® Denture Base Resin

FDA UDI

Class II (US FDA UDI)

by Dentsply International

Identity

Trade Name
DENTSPLY TruByte® Characterized Lucitone® Denture Base Resin FDA UDI
Generic Name
Medicine bottle FDA UDI
Device Name
DENTSPLY TruByte® Characterized Lucitone® Denture Base Resin - Single Unit Packaging 50 Unit Pkg Reddish Pink FDA UDI
Model / Reference
686043 FDA UDI
Description
DENTSPLY TruByte® Characterized Lucitone® Denture Base Resin - Single Unit Packaging 50 Unit Pkg Reddish Pink FDA UDI

Identifiers

Catalog Number
686043 FDA UDI
Primary DI / UDI-DI
D0026860431 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Medicine bottle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3760 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Weight — 21 Gram FDA UDI
Total Volume — 430 Milliliter FDA UDI

Category: Medicine bottle

DENTSPLY TruByte® Characterized Lucitone® Denture Base Resin by Dentsply International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medicine bottle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dentsply International

Sources (1)

  • FDA UDI 844e7db5-7ce9-4d5d-b865-6e405164ea2e 37 fields · synced May 30, 2026