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Clinpro™

FDA UDI

Class II (US FDA UDI)

by 3m Company

Identity

Trade Name
Clinpro™ FDA UDI
Generic Name
Dental unfilled resin sealant/coating FDA UDI
Device Name
3M™ ESPE™ Clinpro™ Sealant Bottle Intro Kit, 12621 FDA UDI
Model / Reference
12621 FDA UDI
Description
3M™ ESPE™ Clinpro™ Sealant Bottle Intro Kit, 12621 FDA UDI

Identifiers

Catalog Number
12621 FDA UDI
Primary DI / UDI-DI
30605861010758 FDA UDI
FDA Product Code
EBC FDA UDI
KLE FDA UDI
GMDN Term
Dental unfilled resin sealant/coating FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3765 FDA UDI
872.3200 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

Category: Dental etching solutionDental unfilled resin sealant/coating

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

Similar devices

Also classified as Dental unfilled resin sealant/coating.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI 58e96030-f607-4816-9d7b-3c6d10525669 35 fields · synced May 30, 2026