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Vilex Fibula Drill

FDA UDI

Class I (US FDA UDI)

by Vilex, Inc.

Identity

Trade Name
Vilex Fibula Drill FDA UDI
Generic Name
Fluted surgical drill bit, single-use, non-sterile FDA UDI
Device Name
Drill, Fibula 2.5x245mm FDA UDI
Model / Reference
ZF-DRLL-25 FDA UDI
Description
Drill, Fibula 2.5x245mm FDA UDI

Identifiers

Catalog Number
ZF-DRLL-25 FDA UDI
Primary DI / UDI-DI
00841731122001 FDA UDI
510(k) Number
K151456 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Fluted surgical drill bit, single-use, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Fluted surgical drill bit, single-use, non-sterile

Vilex Fibula Drill by Vilex, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluted surgical drill bit, single-use, non-sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vilex, Inc.

Sources (1)

  • FDA UDI c38c32fb-e53d-44ee-ada6-ec9a74ac72fc 35 fields · synced May 30, 2026