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Dental City

FDA UDI

Class I (US FDA UDI)

by Icp, Inc.

Identity

Trade Name
Dental City FDA UDI
Generic Name
Dentifrice FDA UDI
Model / Reference
40-380M FDA UDI

Identifiers

Primary DI / UDI-DI
D77140380M1 FDA UDI
FDA Product Code
EJR FDA UDI
GMDN Term
Dentifrice FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6030 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dentifrice

Dental City is a cutting-edge, public-use dental device designed to provide effective polishing and cleaning of teeth with a unique Dentifrice formula. Developed by ICP, INC., this device is intended for general oral hygiene use in individuals of all ages and is not intended for implantation. It is a single-use, labeled as no MRI safety information, and is available for commercial distribution.

Similar devices

Also classified as Dentifrice.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Icp, Inc.

Sources (1)

  • FDA UDI 24479a9c-7460-40e1-bbf2-7a36bb8f7f8c 32 fields · synced Sep 17, 2026