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Ribbond Wetting Resin

FDA UDI

Class II (US FDA UDI)

by Ribbond, Inc.

Identity

Trade Name
Ribbond Wetting Resin FDA UDI
Generic Name
Dentine bonding agent/set FDA UDI
Device Name
light curing, unfilled dental adhesive used as an interface between Ribbond fibers and composite. FDA UDI
Model / Reference
1 FDA UDI
Description
light curing, unfilled dental adhesive used as an interface between Ribbond fibers and composite. FDA UDI

Identifiers

Catalog Number
RESIN FDA UDI
Primary DI / UDI-DI
D758RR0 FDA UDI
FDA Product Code
KLE FDA UDI
GMDN Term
Dentine bonding agent/set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3200 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dentine bonding agent/set

Ribbond Wetting Resin by Ribbond, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dentine bonding agent/set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ribbond, Inc.

Sources (1)

  • FDA UDI f7a0fefe-7ab0-41e5-90d6-79eddcc399ca 36 fields · synced May 31, 2026