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Trefoil™

FDA UDI

Class I (US FDA UDI)

by Nobel Biocare AG

Identity

Trade Name
Trefoil™ FDA UDI
Generic Name
Fixture/appliance dental drill bit, single-use FDA UDI
Device Name
Twist Drill Trefoil™ 4.4x11.5-13mm FDA UDI
Model / Reference
38338 FDA UDI
Description
Twist Drill Trefoil™ 4.4x11.5-13mm FDA UDI

Identifiers

Catalog Number
38338 FDA UDI
Primary DI / UDI-DI
07332747105186 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Fixture/appliance dental drill bit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 13.000 Millimeter FDA UDI
Outer Diameter — 4.400 Millimeter FDA UDI

Category: Fixture/appliance dental drill bit, single-use

Trefoil™ by Nobel Biocare AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fixture/appliance dental drill bit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nobel Biocare AG

Sources (1)

  • FDA UDI f8f21804-230a-4107-b4c3-ec5ca98a2c6d 36 fields · synced May 30, 2026