Lynal® Tissue Conditioner and Temporary Reliner

FDA UDI

Class II (US FDA UDI)

by Dentsply International

Identity

Trade Name: Lynal® Tissue Conditioner and Temporary Reliner FDA UDI
Generic Name: Denture reliner, soft, professional FDA UDI
Device Name: Lynal® Tissue Conditioner & Temporary Reliner Package FDA UDI
Model / Reference: 653006 FDA UDI
Description: Lynal® Tissue Conditioner & Temporary Reliner Package FDA UDI

Identifiers

Catalog Number: 653006 FDA UDI
Primary DI / UDI-DI: D0026530060 FDA UDI
FDA Product Code: EBI FDA UDI
GMDN Term: Denture reliner, soft, professional 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Total Volume — 90 Milliliter FDA UDI
Weight — 120 Gram FDA UDI

Category: Denture reliner, soft, professional

Lynal® Tissue Conditioner and Temporary Reliner by Dentsply International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Dentsply International

Sources (1)

FDA UDI 5bdeace2-ffa5-4557-95e5-68e5bf834e3e 37 fields · synced Jun 8, 2026