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Flexacryl Hard Liquid

FDA UDI

Class II (US FDA UDI)

by Lang Dental Manufacturing Company, Inc.

Identity

Trade Name
FLEXACRYL HARD LIQUID FDA UDI
Generic Name
Denture reliner, soft, professional FDA UDI
Device Name
DENTURE RELINE ACRYLIC RESIN LIQUID FDA UDI
Model / Reference
118 ML FDA UDI
Description
DENTURE RELINE ACRYLIC RESIN LIQUID FDA UDI

Identifiers

Catalog Number
0903R FDA UDI
Primary DI / UDI-DI
D6500903R0 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Denture reliner, soft, professional

Flexacryl Hard Liquid by Lang Dental Manufacturing Company, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Denture reliner, soft, professional.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6fc15af3-7966-488f-98d2-7b108eb4ccd2 34 fields · synced May 31, 2026