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Cybercut

FDA UDI

Class I (US FDA UDI)

by Lares Research, Inc.

Identity

Trade Name
Cybercut FDA UDI
Generic Name
Carbide dental bur, single-use FDA UDI
Device Name
RA CARBIDE 8 - 10 PACK FDA UDI
Model / Reference
RA CARBIDE 8 FDA UDI
Description
RA CARBIDE 8 - 10 PACK FDA UDI

Identifiers

Catalog Number
LC0031 FDA UDI
Primary DI / UDI-DI
D950LC00311 FDA UDI
FDA Product Code
EJL FDA UDI
GMDN Term
Carbide dental bur, single-use 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

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: Carbide dental bur, single-use

Cybercut by Lares Research, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Carbide dental bur, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 382d8d01-08ec-470f-8c59-0973514bd709 35 fields · synced Jun 8, 2026