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3m™ Espe™

FDA UDI

Class I (US FDA UDI)

by 3m Company

Identity

Trade Name
3M™ ESPE™ FDA UDI
Generic Name
Dental matrix band, single-use FDA UDI
Device Name
3M™ ESPE™ Pedodontic Anterior Strip Crown Form, Upper Left Central, Size 4, 914004 FDA UDI
Model / Reference
914004 FDA UDI
Description
3M™ ESPE™ Pedodontic Anterior Strip Crown Form, Upper Left Central, Size 4, 914004 FDA UDI

Identifiers

Catalog Number
914004 FDA UDI
Primary DI / UDI-DI
30605861026698 FDA UDI
FDA Product Code
KCQ FDA UDI
GMDN Term
Dental matrix band, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6570 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental matrix band, single-use

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

Similar devices

Also classified as Dental matrix band, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI c02b4fca-2f16-4073-8c9d-e4539597b4b4 35 fields · synced May 31, 2026