← Back to catalogue

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
T&F CARBIDE FG 7379, 12 BLADE, 25 BAG FDA UDI
Model / Reference
T&F CARBIDE FG 7379, 12 BLADE FDA UDI
Description
T&F CARBIDE FG 7379, 12 BLADE, 25 BAG FDA UDI

Identifiers

Catalog Number
LC0052 FDA UDI
Primary DI / UDI-DI
D950LC00521 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI f9de237c-31eb-425b-b2c4-ba88eb9582bd 35 fields · synced May 30, 2026