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Drill Wire Kit

FDA UDI

Class I (US FDA UDI)

by Curvafix Inc

Identity

Trade Name
Drill Wire Kit FDA UDI
Generic Name
Orthopaedic guidewire, single-use FDA UDI
Device Name
A single use kit, composed of a sterile packaged Drill Wire and Exchange Tube, that is used during a surgical procedure for the placement of the CurvaFix IM Implant. FDA UDI
Model / Reference
DWK-001 FDA UDI
Description
A single use kit, composed of a sterile packaged Drill Wire and Exchange Tube, that is used during a surgical procedure for the placement of the CurvaFix IM Implant. FDA UDI

Identifiers

Catalog Number
DWK-001 FDA UDI
Primary DI / UDI-DI
10855068008126 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic guidewire, single-use 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

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

Yes

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

Category: Orthopaedic guidewire, single-use

Drill Wire Kit by Curvafix Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic guidewire, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Curvafix Inc

Sources (1)

  • FDA UDI c9bebaf0-0459-40c3-8427-f21734417f4d 35 fields · synced May 30, 2026