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Edenta

FDA UDI

Class I (US FDA UDI)

by Edenta Etablissement

Identity

Trade Name
EDENTA FDA UDI
Generic Name
Carbide dental bur, reusable FDA UDI
Device Name
Parallel milling cutter bevel grinding FDA UDI
Model / Reference
2666F.123.015 FDA UDI
Description
Parallel milling cutter bevel grinding FDA UDI

Identifiers

Primary DI / UDI-DI
E3122666F1230151 FDA UDI
FDA Product Code
EJL FDA UDI
GMDN Term
Carbide dental bur, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3240 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

No

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

Yes

FDA UDI

Category: Carbide dental bur, reusable

Edenta by Edenta Etablissement — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Carbide dental bur, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2c3c5383-7a75-4140-b3d2-68a37abaec43 33 fields · synced Jun 1, 2026