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GC Fuji PLUS®

FDA UDI

Class II (US FDA UDI)

by Gc America Inc.

Identity

Trade Name
GC Fuji PLUS® FDA UDI
Generic Name
Dental etching solution FDA UDI
Device Name
GC Fuji PLUS® Conditioner btl. (6.5 mL) FDA UDI
Model / Reference
000221 FDA UDI
Description
GC Fuji PLUS® Conditioner btl. (6.5 mL) FDA UDI

Identifiers

Catalog Number
000221 FDA UDI
Primary DI / UDI-DI
D0470002211 FDA UDI
510(k) Number
K946100 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Dental etching solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3275 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
Weight — 7 Gram FDA UDI

Category: Dental etching solution

GC Fuji PLUS® by Gc America Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental etching solution.

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 2f003bd6-38bd-4506-9361-1969b7f1b1f5 38 fields · synced May 30, 2026