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Vilex Fibula Tool

FDA UDI

Class II (US FDA UDI)

by Vilex, Inc.

Identity

Trade Name
Vilex Fibula Tool FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
Driver, Fibula T10 Long FDA UDI
Model / Reference
ZF-T10 FDA UDI
Description
Driver, Fibula T10 Long FDA UDI

Identifiers

Catalog Number
ZF-T10 FDA UDI
Primary DI / UDI-DI
00841731122032 FDA UDI
510(k) Number
K151456 FDA UDI
FDA Product Code
HSB FDA UDI
HXX FDA UDI
GMDN Term
Surgical screwdriver, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
888.4540 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

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: Surgical screwdriver, reusable

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

Similar devices

Also classified as Surgical screwdriver, reusable.

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 8527b6f9-6702-418f-b789-5172f07e5acd 35 fields · synced May 30, 2026