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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 material cartridge-plunging applicator, two-component, manual FDA UDI
Device Name
3M™ ESPE™ Restorative Dispenser for Capsules, 5707SD FDA UDI
Model / Reference
5707SD FDA UDI
Description
3M™ ESPE™ Restorative Dispenser for Capsules, 5707SD FDA UDI

Identifiers

Catalog Number
5707SD FDA UDI
Primary DI / UDI-DI
30605861039179 FDA UDI
FDA Product Code
EID FDA UDI
GMDN Term
Dental material cartridge-plunging applicator, two-component, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

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 material cartridge-plunging applicator, two-component, manual

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

Similar devices

Also classified as Dental material cartridge-plunging applicator, two-component, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI c9265a3b-a770-41c4-9d3d-4450a4ea83d7 35 fields · synced May 30, 2026