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3M™ Clinpro™

FDA UDI

Class II (US FDA UDI)

by 3m Company

Identity

Trade Name
3M™ Clinpro™ FDA UDI
Generic Name
Dental coating, tooth-desensitizing, professional FDA UDI
Device Name
3M™ Clinpro™ Clear Fluoride Treatment, 7200FF, Flavorless, 0.5 mL Unit Dose, 50/PAC FDA UDI
Model / Reference
7200FF FDA UDI
Description
3M™ Clinpro™ Clear Fluoride Treatment, 7200FF, Flavorless, 0.5 mL Unit Dose, 50/PAC FDA UDI

Identifiers

Catalog Number
7200FF FDA UDI
Primary DI / UDI-DI
10605861083987 FDA UDI
FDA Product Code
LBH FDA UDI
GMDN Term
Dental coating, tooth-desensitizing, professional FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3260 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

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

Yes

FDA UDI

Category: Dental coating, tooth-desensitizing, professional

3M™ Clinpro™ by 3m Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental coating, tooth-desensitizing, professional.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI 4d02e55d-94d7-4b67-9bf0-89b56d23fa83 35 fields · synced Jun 1, 2026