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Filtek™

FDA UDI

Class II (US FDA UDI)

by 3m Company

Identity

Trade Name
Filtek™ FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
3M™ ESPE™ Esthetic Restoration Sample Kit, 6029CP FDA UDI
Model / Reference
6029CP FDA UDI
Description
3M™ ESPE™ Esthetic Restoration Sample Kit, 6029CP FDA UDI

Identifiers

Catalog Number
6029CP FDA UDI
Primary DI / UDI-DI
30605861060838 FDA UDI
FDA Product Code
KLE FDA UDI
EBF FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3200 FDA UDI
872.3690 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

No

FDA UDI

Category: Dental composite resinDentine bonding agent/set

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

Similar devices

Also classified as Dentine bonding agent/set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI 109db67f-c1c1-48f2-84d6-17cc85adbcfa 35 fields · synced Jun 8, 2026