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NIC or SUPERLINE

FDA UDI

Class I (US FDA UDI)

by Shenzhen Superline Technology Co., Ltd.

Identity

Trade Name
NIC or SUPERLINE FDA UDI
Generic Name
Diamond dental bur, reusable FDA UDI
Device Name
The product is used with dental motors, it is intended for cutting, trim and finish natural and engineered dental materials during various dental procedures. FDA UDI
Model / Reference
Cylinder Flat End FDA UDI
Description
The product is used with dental motors, it is intended for cutting, trim and finish natural and engineered dental materials during various dental procedures. FDA UDI

Identifiers

Primary DI / UDI-DI
06944835190571 FDA UDI
FDA Product Code
DZP FDA UDI
GMDN Term
Diamond dental bur, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4535 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Diamond dental bur, reusable

NIC or SUPERLINE by Shenzhen Superline Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Diamond dental bur, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ad7d317a-b913-4e92-8e42-fde95822ced2 34 fields · synced May 30, 2026