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G-aenial™

FDA UDI

Class II (US FDA UDI)

by Gc America Inc.

Identity

Trade Name
G-aenial™ FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
G-aenial™Universal Flo A4, 1 syringe (2 mL/3.4 g per syringe) and 15 dispensing tips FDA UDI
Model / Reference
004206 FDA UDI
Description
G-aenial™Universal Flo A4, 1 syringe (2 mL/3.4 g per syringe) and 15 dispensing tips FDA UDI

Identifiers

Catalog Number
004206 FDA UDI
Primary DI / UDI-DI
14548161323239 FDA UDI
510(k) Number
K091388 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 2 Milliliter FDA UDI

Category: Dental composite resin

G-aenial™ by Gc America Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gc America Inc.

Sources (1)

  • FDA UDI 9a892a26-0c10-4fdd-8e54-d24cb09d4a08 38 fields · synced May 29, 2026