Dental City

FDA UDI

Class I (US FDA UDI)

by Icp, Inc.

Identity

Trade Name: Dental City FDA UDI
Generic Name: Dental material application tool, single-use FDA UDI
Device Name: Dental City Micro Applicator Superfine White 100/Tube FDA UDI
Model / Reference: 53-1000 FDA UDI
Description: Dental City Micro Applicator Superfine White 100/Tube FDA UDI

Identifiers

Primary DI / UDI-DI: D771531000 FDA UDI
FDA Product Code: KXR FDA UDI
GMDN Term: Dental material application tool, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.3140 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Dental material application tool, single-use

Dental City by Icp, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Icp, Inc.

Sources (1)

FDA UDI 2179539d-f76b-4b22-b601-869ce0477785 33 fields · synced Jun 1, 2026