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Anterior BBA

FDA UDI

Class I (US FDA UDI)

by Cosmedent, Inc.

Identity

Trade Name
Anterior BBA FDA UDI
Generic Name
Dental restoration carver, resin FDA UDI
Model / Reference
100G3 FDA UDI

Identifiers

Primary DI / UDI-DI
D779100G3 FDA UDI
FDA Product Code
EJB FDA UDI
GMDN Term
Dental restoration carver, resin FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental restoration carver, resin

Anterior BBA by Cosmedent, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental restoration carver, resin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cosmedent, Inc.

Sources (1)

  • FDA UDI 82ba9e17-af99-41b6-ae3b-881bfbcb4e11 32 fields · synced May 30, 2026