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Ribbond Securing Composite

FDA UDI

Class II (US FDA UDI)

by Ribbond, Inc.

Identity

Trade Name
Ribbond Securing Composite FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
High viscosity flowable composite. Light cured micro hybrid. FDA UDI
Model / Reference
1 FDA UDI
Description
High viscosity flowable composite. Light cured micro hybrid. FDA UDI

Identifiers

Catalog Number
TIPS FDA UDI
Primary DI / UDI-DI
D046CC0 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 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

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: Dental composite resin

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

Similar devices

Also classified as Dental composite resin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ribbond, Inc.

Sources (1)

  • FDA UDI 4b1417f9-71a7-48a4-a897-92022f64ad79 36 fields · synced May 30, 2026